Potassium Iodide inactive ingredients by manufacturer
Wondering whether your Potassium Iodide has lactose, gluten, soy, a dye or gelatin in it? The medicine is the same, but the fillers, coatings and colors differ from one company to the next. This page shows what each Potassium Iodide product's FDA label lists, so you can find a version that leaves out what you avoid and ask your pharmacist for it by its NDC.
We have read the FDA labels of 10 of the 10 current Potassium Iodide products on the market today, from 9 companies listing it with the FDA, and lined them up side by side.
Ask about your bottle
Is there something in your Potassium Iodide? Ask in plain words.
Name the company, strength or the NDC on your bottle and the ingredient you avoid. The answer comes only from the FDA labels on this page.
Answers are drawn from the FDA label data on this page and checked against it. They are not medical advice: confirm with your pharmacist before relying on them.
The short answer
Which Potassium Iodide products list lactose, a gluten source, soy, dyes or gelatin?
-
LactoseDiffers by manufacturer
2 of 10 checked products list lactose; 8 do not. See the products
-
Wheat or gluten sourceNo checked product
No checked Potassium Iodide product lists a wheat or gluten source.
-
SoyNo checked product
No checked Potassium Iodide product lists soy.
-
Synthetic dyesDiffers by manufacturer
1 of 10 checked products list synthetic dyes; 9 do not. See the products
Does not list it Anbex Atlantic Biologicals Avondale Bryant Ranch Prepack BTG International Inc BTG International Inc. Emerald Therapeutics NivagenLists it Mission Pharmacal -
GelatinNo checked product
No checked Potassium Iodide product lists gelatin.
Also listed by some products: Propylene glycol 1 of 10 Sugar 1 of 10
Find a version without it
Every current Potassium Iodide product and what its label lists
| Product | Lists | Inactive ingredients on the label |
|---|---|---|
| Anbex Inc. 2 products | ||
| 65 mg tabletNDC 51803-0002-01 | None of these listed |
Show 4 ingredientsCELLULOSE, MICROCRYSTALLINE, MAGNESIUM STEARATE, SILICON DIOXIDE, SODIUM THIOSULFATE ANHYDROUS |
| 130 mg tabletNDC 51803-0001-01 | None of these listed |
Show 4 ingredientsCELLULOSE, MICROCRYSTALLINE, MAGNESIUM STEARATE, SILICON DIOXIDE, SODIUM THIOSULFATE ANHYDROUS |
| Atlantic Biologicals Corp. 1 product | ||
| 1 g/mL oral solutionNDC 17856-0114-01 | None of these listed |
Show 1 ingredientSODIUM THIOSULFATE |
| Avondale Pharmaceuticals, LLC 1 product | ||
| 1 g/mL oral solutionNDC 71740-0112-30 | None of these listed |
Show 1 ingredientsodium thiosulfate |
| Bryant Ranch Prepack 1 product | ||
| 1 g/mL oral solutionNDC 72162-2423-02 | None of these listed |
Show 1 ingredientSODIUM THIOSULFATE |
| BTG International Inc 1 product | ||
| 130 mg tabletNDC 50633-0920-20 | Lactose |
Show 3 ingredientsLACTOSE, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE |
| BTG International Inc. 1 product | ||
| 65 mg tabletNDC 50633-0910-20 | Lactose |
Show 3 ingredientsLACTOSE, UNSPECIFIED FORM, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE |
| Emerald Therapeutics, LLC 1 product | ||
| 1 g/mL oral solutionNDC 72919-0728-30 | None of these listed |
Show 1 ingredientSODIUM THIOSULFATE |
| Mission Pharmacal Company 1 product | ||
| 65 mg/mL oral solutionNDC 00178-0314-30 | Synthetic dyes Propylene glycol Sugar (sucrose, dextrose) |
Show 9 ingredientsBLACK RASPBERRY, FD&C BLUE NO. 1, FD&C RED NO. 40, METHYLPARABEN, PROPYLENE GLYCOL, PROPYLPARABEN, SACCHARIN SODIUM, SUCROSE, WATER |
| Nivagen Pharmaceuticals, Inc. 1 product | ||
| 1 g/mL oral solutionNDC 75834-0280-08 | None of these listed |
Show 1 ingredientSODIUM THIOSULFATE |
A product with none of these listed is not certified to be without them: the label says what the manufacturer declared, and the source of a starch or a flavor is often not stated. The companies are the FDA's labelers, which include repackagers and distributors selling another company's product under their own label. The NDC opens the product's own page, with the full label and its inactive-ingredient notes.
Potassium Iodide without lactose
Lactose: milk sugar; a concern with lactose intolerance or a milk allergy. 2 of 10 checked products list lactose; 8 do not.
Does not list lactose
- Anbex: 65 mg tablet, 130 mg tablet
- Atlantic Biologicals: 1 g/mL oral solution
- Avondale: 1 g/mL oral solution
- Bryant Ranch Prepack: 1 g/mL oral solution
- Emerald Therapeutics: 1 g/mL oral solution
- Mission Pharmacal: 65 mg/mL oral solution
- Nivagen: 1 g/mL oral solution
Lists lactose
- BTG International Inc: 130 mg tablet
- BTG International Inc.: 65 mg tablet
Potassium Iodide without synthetic dyes
Synthetic dyes: FD&C or D&C colorants and their aluminum lakes. 1 of 10 checked products list synthetic dyes; 9 do not.
Does not list synthetic dyes
- Anbex: 65 mg tablet, 130 mg tablet
- Atlantic Biologicals: 1 g/mL oral solution
- Avondale: 1 g/mL oral solution
- Bryant Ranch Prepack: 1 g/mL oral solution
- BTG International Inc: 130 mg tablet
- BTG International Inc.: 65 mg tablet
- Emerald Therapeutics: 1 g/mL oral solution
- Nivagen: 1 g/mL oral solution
Lists synthetic dyes
- Mission Pharmacal: 65 mg/mL oral solution
Potassium Iodide without propylene glycol
Propylene glycol: A solvent in liquids and capsules; a concern in kidney disease, for infants, and at high doses. 1 of 10 checked products list propylene glycol; 9 do not.
Does not list propylene glycol
- Anbex: 65 mg tablet, 130 mg tablet
- Atlantic Biologicals: 1 g/mL oral solution
- Avondale: 1 g/mL oral solution
- Bryant Ranch Prepack: 1 g/mL oral solution
- BTG International Inc: 130 mg tablet
- BTG International Inc.: 65 mg tablet
- Emerald Therapeutics: 1 g/mL oral solution
- Nivagen: 1 g/mL oral solution
Lists propylene glycol
- Mission Pharmacal: 65 mg/mL oral solution
Potassium Iodide without sugar (sucrose or dextrose)
Sugar (sucrose, dextrose): A consideration in diabetes, mostly in liquids and chewables. 1 of 10 checked products list sugar (sucrose or dextrose); 9 do not.
Does not list sugar (sucrose or dextrose)
- Anbex: 65 mg tablet, 130 mg tablet
- Atlantic Biologicals: 1 g/mL oral solution
- Avondale: 1 g/mL oral solution
- Bryant Ranch Prepack: 1 g/mL oral solution
- BTG International Inc: 130 mg tablet
- BTG International Inc.: 65 mg tablet
- Emerald Therapeutics: 1 g/mL oral solution
- Nivagen: 1 g/mL oral solution
Lists sugar (sucrose or dextrose)
- Mission Pharmacal: 65 mg/mL oral solution
At the pharmacy counter
How to use this at the pharmacy counter
- Pick the company whose list suits you and copy the NDC from the table. Many pharmacies order from wholesalers that carry several companies' versions and can request a particular one if you ask before the prescription is filled; some buy from one contracted source only, and a few insurance plans cover only certain NDCs, so ask the pharmacist to check.
- Treat "does not list" as exactly that. The label is what the manufacturer declared; a flavor or a starch may have an unstated source, and lines change. For celiac disease or a serious allergy, ask the manufacturer's medical information line for a written statement about the lot you have.
- Check the bottle each refill. A different company usually means a different shape, color and inactive-ingredient list; the pharmacist can tell you who made it, and the two-NDC comparison shows the difference line by line.
- If you need one company's version kept constant, ask your prescriber to write that company or the NDC on the prescription and tell the pharmacy you need it held. Rules vary by state and plan, so confirm with the pharmacist.
Common questions about Potassium Iodide inactive ingredients
Is Potassium Iodide gluten-free?
Does Potassium Iodide contain lactose?
Does Potassium Iodide contain soy?
Is there a dye-free Potassium Iodide?
Does Potassium Iodide contain gelatin?
Why do the inactive ingredients differ between manufacturers?
Can my pharmacy give me a specific manufacturer's version?
How current is this list?
Sources: the products are the finished Potassium Iodide products in the FDA's current NDC directory (openFDA), as of October 5, 2026; each inactive-ingredient list is the manufacturer's FDA Structured Product Label via DailyMed, as our label sync last read it. The concern groups are HelloPharmacist's classification of the names the label declares. Educational information only, not medical advice; confirm with your pharmacist before relying on a list. ← Back to the Potassium Iodide guide