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

Gluten Free Non Food Products


eblue

Recommended Posts

eblue Apprentice

So, being a newbie and all (diagnosed a month ago) I am still learning a lot. What types of non food products are safe? I know that you can only get glutened by ingesting it, but I am pretty bad about touching my face/lips often throughout the day and I really prefer purchasing gluten free products to be extra safe. Can anyone help me out on ideas for the following items? Oh, and preferably stuff I can buy at walmart/CVS type places. I really don't want to spend a fortune if I don't have to. I have already bought Dove shampoo/ conditioner and lotion :)

 

Hand soap

 

hand sanitizer

 

lip balm

 

lip stick

 

liquid foundation

 

and anything else that you have found to be gluten-free!

 

Oh, and also, what Over the counter pain medications are safe? I dont like to take them often, but ocasionally I do take them. 

 

Thanks!! I am so thankful for all of yall on this forum. You have really helped a newbie out A LOT. Thank you thank you thank you. Adjusting to a gluten-free lifestyle is overwhelming. Yall have helped a ton!! Hugs!


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



Celiac.com Sponsor (A8-M):



Adalaide Mentor

For hand soap we keep Softsoap in the house for kitchen and bathrooms. I just get one each of a certain kind I like and a huge refill thing and keep refilling all the little ones til its out. Then I decide if I want to change smells or not.

 

I'm too lazy to go check my hand sanitizer, but I think its name brand something or other. *shrug*

 

I use EOS for my lip balm/chapstick or whatever. I love love love that stuff. My husband balked at the price of it, but then again I'm the first person he has ever known who will use an entire thing of lip balm and not have it go mysteriously missing. So I'll pay however much I want for mine. :P I also use the same brand of hand lotion that I keep in my purse, it is small and handy and slips in a jeans pocket for when I don't want to have my purse with me.

 

I do not wear makeup, so I'm no help there. I used to, and I've seen some say that they don't particularly worry about it but I'm also a toucher. I would worry about it if it were me. I also am quite in the habit of getting (just a little) face wash in my mouth. I know this because I use a homemade face scrub and can always taste the ingredients in it just a teensy bit. If I can taste that, I know that whatever I had on my face is getting in my mouth too. I'm sure someone will have lots of good makeup suggestions.

 

I buy lots of generic drugs at Walgreens. Some packages say gluten free right on them, some don't. I just go during East coast business hours with a cell phone and start calling to be sure of what I am taking. Because things can change at any time, it is important to make these calls every time you purchase a generic. With name brands, I don't know and they may just be safe or not, but I'm not about to waste my money on a name brand.

 

And it becomes less overwhelming and more second nature faster than you think possible. Hang in there!

kareng Grand Master

I have found a lot less things contain gluten than some of these internet sites lead you to believe.  I have found gluten the most prevalent in hair products. Target generic brand Advil and some other OTC meds say gluten-free on the box.. 

Adalaide Mentor

OMG hair products are the root of all evil for gluten. Seriously. I eventually gave up calling people because every product I ever loved either has gluten, or has some stupid company that treats us like complete crap and I won't give my money to them. (The "you won't eat our shampoo and besides we have propriety stuff blah blah blah.." Well no crap I won't eat your shampoo and if you took 10 seconds to actually read the email I sent you would see that it says something about accidental ingestion morons... thanks, I'll keep my money jerkwads.) I eventually gave up and just make my own shampoo at home and use a vinegar rinse, or if I'm feeling lazy I just so shampoo free and do the baking soda method. My hair has never been softer.

 

I also meant to mention with the EOS stuff, I know their shaving cream says oatmeal on it but someone said once that it actually gluten free. This led to me emailing and calling them about it and they told me both times that it is actually gluten free, gluten free oats and all. Woohoo! I love the stuff.I only worry about this because I have a terrible (and unsanitary) habit of putting my razor in my mouth when I put cream on my legs. :ph34r:

GlutenStinks15 Explorer

I use Blistex and to my knowledge it's gluten free - (I wrote the company about 3 months ago when I was diganosed.)

 

I also use the Dove hair products.

  • 2 months later...
KP² Newbie

As far as shampoo, conditioner and other non-color products I just LOVE the Shea Moisture line they carry at CVS, Sally's Beauty Supply & drugstore.com.  I also use a lot of Beauty Control Makeup, but be careful it isn't all gluten-free.The spa line is and so is the Tight Firm & Fill. I do not use any of their lip color or lip treatments however as they all seem to have wheat germ oil in them.    And ain't the hand soap thing a bummer?... I wonder every time I wash my hands in a public restroom if I've just contaminated myself. That one is a booger.

notme Experienced

i buy a giant bar of 'kiss my face' soap and chop it into little bars that i keep in my travel case, and smaller ones to keep in my purse in a baggie.  if they're really little, i just throw it away on my way out of the restroom.  :)


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



Celiac.com Sponsor (A8-M):



  • 10 months later...
SMRI Collaborator

I hope I can post a link but I use this shampoo/conditioner.  I got it before I knew I was diagnosed.  I noticed in passing that the label said gluten-free, but now I guess it makes a difference.  It's also sulfate free but unlike most sulfate free shampoos, it lathers great!!  You only need a very small amount, pea sized for medium length hair.  I have the mint conditioner and it smells so good!!!  Open Original Shared Link .  It's expensive, $30 or so from the salon.  I got the largest bottle with a pump, I've had it since last October and have used maybe 1/2 a bottle.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,948
    • Most Online (within 30 mins)
      7,748

    Stephanie94
    Newest Member
    Stephanie94
    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

    • Jacki Espo
      This happened to me as well. What’s weirder is that within a couple hours of taking paxlovid it subsided. I thought maybe I got glutened but after reading your post not so sure. 
    • Mari
      Hi Tiffany. Thank you for writing your dituation and  circumstancesin such detail and so well writte, too. I particularly noticed what you wrote about brain for and feeling like your brain is swelling and I know from my own experiences that's how it feel and your brain really does swell and you get migraines.    Way back when I was in my 20s I read a book by 2 MD allergist and they described their patient who came in complaining that her brain, inside her cranium, was swelling  and it happened when she smelled a certain chemical she used in her home. She kept coming back and insisting her brain actually swelled in her head. The Drs couldn't explain this problem so they, with her permission, performed an operation where they made a small opening through her cranium, exposed her to the chemical then watched as she brain did swell into the opening. The DRs were amazed but then were able to advise her to avoid chemicals that made her brain swell. I remember that because I occasionally had brain fog then but it was not a serious problem. I also realized that I was becoming more sensitive to chemicals I used in my work in medical laboratories. By my mid forties the brain fog and chemicals forced me to leave my  profession and move to a rural area with little pollution. I did not have migraines. I was told a little later that I had a more porous blood brain barrier than other people. Chemicals in the air would go up into my sinused and leak through the blood brain barrier into my brain. We have 2 arteries  in our neck that carry blood with the nutrients and oxygen into the brain. To remove the fluids and used blood from the brain there are only capillaries and no large veins to carry it away so all those fluids ooze out much more slowly than they came in and since the small capillaries can't take care of extra fluid it results in swelling in the face, especially around the eyes. My blood flow into my brain is different from most other people as I have an arterial ischema, adefectiveartery on one side.   I have to go forward about 20 or more years when I learned that I had glaucoma, an eye problem that causes blindness and more years until I learned I had celiac disease.  The eye Dr described my glaucoma as a very slow loss of vision that I wouldn't  notice until had noticeable loss of sight.  I could have my eye pressure checked regularly or it would be best to have the cataracts removed from both eyes. I kept putting off the surgery then just overnight lost most of the vision in my left eye. I thought at the I had been exposed to some chemical and found out a little later the person who livedbehind me was using some chemicals to build kayaks in a shed behind my house. I did not realize the signifance  of this until I started having appointments with a Dr. in a new building. New buildings give me brain fog, loss of balance and other problems I know about this time I experienced visual disturbances very similar to those experienced by people with migraines. I looked further online and read that people with glaucoma can suffer rapid loss of sight if they have silent migraines (no headache). The remedy for migraines is to identify and avoid the triggers. I already know most of my triggers - aromatic chemicals, some cleaning materials, gasoline and exhaust and mold toxins. I am very careful about using cleaning agents using mostly borax and baking powder. Anything that has any fragrance or smell I avoid. There is one brand of dishwashing detergent that I can use and several brands of  scouring powder. I hope you find some of this helpful and useful. I have not seen any evidence that Celiac Disease is involved with migraines or glaucoma. Please come back if you have questions or if what I wrote doesn't make senseto you. We sometimes haveto learn by experience and finding out why we have some problems. Take care.       The report did not mention migraines. 
    • Mari
      Hi Jmartes71 That is so much like my story! You probably know where Laytonville is and that's where I was living just before my 60th birthday when the new Dr. suggested I could have Celiacs. I didn't go on a gluten challange diet before having the Celiac panel blood test drawn. The results came back as equivical as one antibody level was very high but another, tissue transaminasewas normal. Itdid show I was  allergic to cows milk and I think hot peppers. I immediately went gluten free but did not go in for an endoscopy. I found an online lab online that would do the test to show if I had a main celiac gene (enterolab.com). The report came back that I had inherited a main celiac gene, DQ8, from one parent and a D!6 from the other parent. That combination is knows to sym[tons of celiac worse than just inheriting one main celiac gene. With my version of celiac disease I was mostly constipated but after going gluten-free I would have diarrhea the few times I was glutened either by cross contamination or eating some food containing gluten. I have stayed gluten-free for almost 20 years now and knew within a few days that it was right for me although my recovery has been slow.   When I go to see a  medical provide and tell them I have celiacs they don't believe me. The same when I tell them that I carry a main celiac gene, the DQ8. It is only when I tell them that I get diarrhea after eating gluten that they realize that I might have celiac disease. Then they will order th Vitamin B12 and D3 that I need to monitor as my B12 levels can go down very fast if I'm not taking enough of it. Medical providers haven't been much help in my recovery. They are not well trained in this problem. I really hope this helps ypu. Take care.      
    • knitty kitty
    • DebJ14
×
×
  • 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.