Jump to content
  • Welcome to Celiac.com!

    You have found your celiac tribe! Join us and ask questions in our forum, share your story, and connect with others.




  • Celiac.com Sponsor (A1):



    Celiac.com Sponsor (A1-M):


  • Get Celiac.com Updates:
    Support Our Content
    eNewsletter
    Donate

Werther's Original Hard Candy


2Boys4Me

Recommended Posts

2Boys4Me Enthusiast

Does anyone know if Werther's original is gluten-free? The ingredients look okay, but I can't find a website or phone number to confirm it.

Thanks.


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



snapple Apprentice

Hello! I just did an online search and found the website. Werther's is owned by Storck; I do not believe that it is based in the US. If you want to contact them here is the website to submit your question: Open Original Shared Link

Hope this helps!

num1habsfan Rising Star
Does anyone know if Werther's original is gluten-free? The ingredients look okay, but I can't find a website or phone number to confirm it.

Thanks.

I eat them all the time, actually use then as coughdrops, and have NEVER had an issue with them! But I could be wrong...

~lisa~

blueeyedmanda Community Regular

I have a cup of them sitting on my desk, no problems here either

  • 1 year later...
Christian Newbie

In answer to the question as to whether Werther's candies are gluten free................the ingredients on the back of the bag indicate that there is wheat in the candies.

psawyer Proficient

This discussion began in the summer of 2006. What was true of ingredients at that time may no longer be true. Formulas change all the time.

Werther's is a brand which applies to a number of candies. Christian, which ones specifically do you mean? The original poster asked about Werther's Original, which I have also eaten without incident, although not recently.

This should also be a reminder to always read the ingredient list. I admit I don't always do it, but whenever a package looks different than the last one, I read. If it is something that I haven't bought in a while, I read. If in any doubt, I read.

darlindeb25 Collaborator

I have not read the package in the last few months, but I do know, they did change the ingredients and included wheat. That's when I quit keeping them in my desk for that occasional throat tickle. I was very disappointed when they changed the ingredients.

This is their statement as of July 07:

Werther's

7/07

The following somewhat confusing letter was received 6/19/07 from Michael Phillips from the STORCK manufacturing company (312-467-5700):

"Based on the guidelines of the German association for celiac disease, products with a gluten content less than 200ppm can be named as 'Gluten Free'.

The 200 ppm limit is also a well known international guidance level based on the codex alimentarius. The following products fall below this limit:

Werther's Original Hard

Werther's Orinal Hard Sugar Free

Werther's Orignal Chewy

Werther's Chocolates

Riesen

Mamba

Milkfuls

Toffifay

Unfortunately, we cannot say that our products are completely gluten free because some of our products may contain small amounts of wheat gluten. So to be sure, and to avoid becoming ill, we recommend that you only purchase those products that you know positively are 100% gluten free."


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



  • 1 year later...
Roda Rising Star

Here is a link to their ingredients. I was wondering this myself. I want to eat one since hubby brought a bag home. I believe they don't lable it gluten free because of the glucose syrup they use sometimes comes from wheat. I have read that even glucose syrup made from gluten grains is safe because of the high degree of processing. I have eaten the cadburry eggs and they have it in too without any problem so I think I'll try and see.

Open Original Shared Link

  • 1 year later...
JillianLindsay Enthusiast

I don't see the Werther's Chocolate Crunch on this site to find the ingredients. I got little Werther's Chocolate Crunch in a cracker at Xmas dinner and am wondering if they're safe to eat. They don't have the ingredients on the wrapper and I can't seem to find them online! Anyone have up-to-date info on this?

Thanks :)

Jillian

P.S. -- if it's Canadian info, that would be even better! Thanks~

Here is a link to their ingredients. I was wondering this myself. I want to eat one since hubby brought a bag home. I believe they don't lable it gluten free because of the glucose syrup they use sometimes comes from wheat. I have read that even glucose syrup made from gluten grains is safe because of the high degree of processing. I have eaten the cadburry eggs and they have it in too without any problem so I think I'll try and see.

Open Original Shared Link

karen577 Newbie

Does anyone know if Werther's original is gluten-free? The ingredients look okay, but I can't find a website or phone number to confirm it.

Thanks.

I read this forum earlier today and decided to take the risk and try a couple Werther's. I had a skin reaction later that day and I suspect it was from the candies since they were the only food I had today that was not guaranteed gluten free.

MelindaLee Contributor

Just from the name "crunch" I would be suspicious. Usually the crunch is either cookie or crispies, both of which aren't safe. I did find them on the internet, the crunch is from nuts. Unfortunately the orginal toffee, which is also part of it, has Wheat as a possible ingreadient (Wheat or corn). I don't think I would try them. <_<

  • 10 months later...
gputman Newbie

The allergy warnings on the sugar free ones don't contain a wheat warning

  • 10 months later...
Owlmuse Rookie

Has anyone settled this yet? There I was sucking my delicious werthers' hard candy only to see it has glucose syrup made from wheat in it! I was horrifid!! I've since done some research on glucose syrup but I'm still very confused! I've found that according to the werther's site, gluten free living magazine site and (in another post) the Australian New zelend equivalent of the FDA and celiac foundation that its fine. Yet I've seen numberpus posts by people who say they have problems. It seems to be a real issue abroad as glucose syrup in the states is made from corn. It just happens that werther's are from Germany. I'm a silent celiac and can't tell on my own what's causing a problem. Has anyone else figured this out? I mean scientifically, not just being scared of the idea or the word 'wheat'.

  • 3 years later...
Amytjeeuh Newbie

I looked for it and found this: Open Original Shared Link
It looks like it's glutenfree!
xxx Amy

RadDecor Newbie

Amytjeeuh:  Thank you for sharing this Werthers' update in 2015.  Appreciate it.

 

  • 3 weeks later...
xjrosie Apprentice

Ingredients: Sugar, Glucose Syrup (from Wheat or Corn), Cream, Condensed Whey, Butter, Cane Sugar Syrup, Salt, Soy Lecithin Emulsifier, Artificial Flavor.

Allergy Information: Contains milk, soybeans and wheat.

 

These are the ingredients for Werther's Original Hard Candies here in the USA. Candies manufactured in other countries may have different ingredients, but these candies ARE NOT gluten free.

Archived

This topic is now archived and is closed to further replies.

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - cristiana replied to Scatterbrain's topic in Sports and Fitness
      5

      Feel like I’m starting over

    2. - knitty kitty replied to Jmartes71's topic in Related Issues & Disorders
      8

      My only proof

    3. - Wheatwacked replied to Jmartes71's topic in Coping with Celiac Disease
      8

      Related issues

    4. - NanceK replied to Jmartes71's topic in Related Issues & Disorders
      8

      My only proof

    5. - Wheatwacked replied to Scatterbrain's topic in Sports and Fitness
      5

      Feel like I’m starting over


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,295
    • Most Online (within 30 mins)
      7,748

    LaniH
    Newest Member
    LaniH
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • cristiana
      Hi @Scatterbrain Thank you for your reply.   Some of these things could be weaknesses, also triggered by stress, which perhaps have come about as the result of long-term deficiencies which can take a long time to correct.   Some could be completely unrelated. If it is of help, I'll tell you some of the things that started in the first year or two, following my diagnosis - I pinned everything on coeliac disease, but it turns out I wasn't always right!  Dizziness, lightheaded - I was eventually diagnosed with cervical dizziness (worth googling, could be your issue too, also if you have neck pain?)  A few months after diagnosis I put my neck out slightly carrying my seven-year-old above my head, and never assigned any relevance to it as the pain at the time was severe but so short-lived that I'd forgotten the connection. Jaw pain - stress. Tinnitus - I think stress, but perhaps exacerbated by iron/vitamin deficiencies. Painful ribs and sacroiliac joints - no idea, bloating made the pain worse. It got really bad but then got better. Irregular heart rate - could be a coincidence but my sister (not a coeliac) and I both developed this temporarily after our second Astra Zeneca covid jabs.   Subsequent Pfizer jabs didn't affect us. Brain fog - a big thing for people with certain autoimmune issues but in my case I think possibly worse when my iron or B12 are low, but I have no proof of this. Insomnia - stress, menopause. So basically, it isn't always gluten.  It might be worth having your vitamins and mineral levels checked, and if you have deficiencies speak to your Dr about how better to address them?    
    • knitty kitty
      @NanceK, I do have Hypersensitivity Type Four reaction to Sulfa drugs, a sulfa allergy.  Benfotiamine and other forms of Thiamine do not bother me at all.  There's sulfur in all kinds of Thiamine, yet our bodies must have it as an essential nutrient to make life sustaining enzymes.  The sulfur in thiamine is in a ring which does not trigger sulfa allergy like sulfites in a chain found in pharmaceuticals.  Doctors are not given sufficient education in nutrition (nor chemistry in this case).  I studied Nutrition before earning a degree in Microbiology.  I wanted to know what vitamins were doing inside the body.   Thiamine is safe and nontoxic even in high doses.   Not feeling well after starting Benfotiamine is normal.  It's called the "thiamine paradox" and is equivalent to an engine backfiring if it's not been cranked up for a while.  Mine went away in about three days.  I took a B Complex, magnesium and added molybdenum for a few weeks. It's important to add a B Complex with all eight essential B vitamins. Supplementing just one B vitamin can cause lows in some of the others and result in feeling worse, too.  Celiac Disease causes malabsorption of all the B vitamins, not just thiamine.  You need all eight.  Thiamine forms including Benfotiamine interact with each of the other B vitamins in some way.  It's important to add a magnesium glycinate or chelate supplement as well.  Forms of Thiamine including Benfotiamine need magnesium to make those life sustaining enzymes.  (Don't use magnesium oxide.  It's not absorbed well.  It pulls water into the intestines and is used to relieve constipation.)   Molybdenum is a trace mineral that helps the body utilize forms of Thiamine.   Molybdenum supplements are available over the counter.  It's not unusual to be low in molybdenum if low in thiamine.   I do hope you will add the necessary supplements and try Benfotiamine again. Science-y Explanation of Thiamine Paradox: https://hormonesmatter.com/paradoxical-reactions-with-ttfd-the-glutathione-connection/#google_vignette
    • Wheatwacked
      Your goal is not to be a good puppet, there is no gain in that. You might want to restart the ones that helped.  It sounds more like you are suffering from malnutrition.  Gluten free foods are not fortified with things like Thiamine (B1), vitamin D, Iodine, B1,2,3,5,6 and 12 as non-gluten free products are required to be. There is a Catch-22 here.  Malnutrition can cause SIBO, and SIBO can worsen malnutrition. Another possibility is side effects from any medication that are taking.  I was on Metformin 3 months before it turned me into a zombi.  I had crippling side effects from most of the BP meds tried on me, and Losartan has many of the side effects on me from my pre gluten free days. Because you have been gluten free, you can test and talk until you are blue in the face but all of your tests will be negative.  Without gluten, you will not create the antigen against gluten, no antigens to gluten, so no small intestine damage from the antigens.  You will need to do a gluten challange to test positive if you need an official diagnosis, and even then, no guaranty: 10 g of gluten per day for 6 weeks! Then a full panel of Celiac tests and biopsy. At a minimum consider vitamin D, Liquid Iodine (unless you have dermatitis herpetiformis and iodine exasperates the rash), and Liquid Geritol. Push for vitamin D testing and a consult with a nutritionist experienced with Celiack Disease.  Most blood tests don't indicate nutritional deficiencies.  Your thyroid tests can be perfect, yet not indicate iodine deficiency for example.  Thiamine   test fine, but not pick up on beriberi.  Vegans are often B12 deficient because meat, fish, poultry, eggs, and dairy are the primary souces of B12. Here is what I take daily.  10,000 IU vitamin D3 750 mg g a b a [   ] 200 mg CoQ10 [   ] 100 mg DHEA [   ] 250 mg thiamine B1 [   ] 100 mg of B2 [   ] 500 mg B5 pantothenic acid [   ] 100 mg B6 [   ] 1000 micrograms B12 n [   ] 500 mg vitamin c [   ] 500 mg taurine [   ] 200 mg selenium   
    • NanceK
      Hi…Just a note that if you have an allergy to sulfa it’s best not to take Benfotiamine. I bought a bottle and tried one without looking into it first and didn’t feel well.  I checked with my pharmacist and he said not to take it with a known sulfa allergy. I was really bummed because I thought it would help my energy level, but I was thankful I was given this info before taking more of it. 
    • Wheatwacked
      Hello @Scatterbrain, Are you getting enough vitamins and minerals.  Gluten free food is not fortified so you may be starting to run low on B vitamins and vitamin D.   By the way you should get your mom checked for celiac disease.  You got it from your mom or dad.  Some studies show that following a gluten-free diet can stabilize or improve symptoms of dementia.  I know that for the 63 years I was eating gluten I got dumber and dumber until I started GFD and vitamin replenishment and it began to reverse.  Thiamine can get used up in a week or two.  Symptoms can come and go with daily diet.  Symptoms of beriberi due to Thiamine deficiency.   Difficulty walking. Loss of feeling (sensation) in hands and feet. Loss of muscle function or paralysis of the lower legs. Mental confusion. Pain. Speech difficulties. Strange eye movements (nystagmus) Tingling. Any change in medications? Last March I had corotid artery surgery (90 % blockage), and I started taking Losartan for blood pressure, added to the Clonidine I was taking already.  I was not recovering well and many of my pre gluten free symptoms were back  I was getting worse.  At first I thought it was caused a reaction to the anesthesia from the surgery, but that should have improved after two weeks.  Doctor thought I was just being a wimp. After three months I talked to my doctor about a break from the Losartan to see if it was causing it. It had not made any difference in my bp.  Except for clonindine, all of the previous bp meds tried had not worked to lower bp and had crippling side effects. One, I could not stand up straight; one wobbly knees, another spayed feet.  Inguinal hernia from the Lisinopril cough.  Had I contiued on those, I was destined for a wheelchair or walker. She said the symptoms were not from Losartan so I continued taking it.  Two weeks later I did not have the strength in hips and thighs to get up from sitting on the floor (Help, I can't get up😨).  I stopped AMA (not recommended).  Without the Losartan, a) bp did not change, after the 72 hour withdrawal from Losartanon, on clonidine only and b) symptoms started going away.  Improvement started in 72 hours.  After six weeks they were gone and I am getting better.  
×
×
  • Create New...

Important Information

NOTICE: This site places This site places cookies on your device (Cookie settings). on your device. Continued use is acceptance of our Terms of Use, and Privacy Policy.