Zileuton inactive ingredients by manufacturer
Wondering whether your Zileuton 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 Zileuton 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 6 of the 6 current Zileuton products on the market today, from 6 companies listing it with the FDA, and lined them up side by side.
Ask about your bottle
Is there something in your Zileuton? 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 Zileuton products list lactose, a gluten source, soy, dyes or gelatin?
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LactoseNo checked product
No checked Zileuton product lists lactose.
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Wheat or gluten sourceNo checked product
No checked Zileuton product lists a wheat or gluten source.
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SoyNo checked product
No checked Zileuton product lists soy.
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Synthetic dyesNo checked product
No checked Zileuton product lists synthetic dyes.
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GelatinNo checked product
No checked Zileuton product lists gelatin.
Also listed by some products: Corn 6 of 6 Titanium dioxide 2 of 6 Propylene glycol 1 of 6 PEG or polysorbate 5 of 6 Sorbitol or mannitol 5 of 6
Find a version without it
Every current Zileuton product and what its label lists
| Product | Lists | Inactive ingredients on the label |
|---|---|---|
| Camber Pharmaceuticals, Inc. 1 product | ||
| 600 mg extended-release tabletNDC 31722-0044-12 | Corn-derived Polyethylene glycol or polysorbate Sorbitol or mannitol |
Show 15 ingredientsCROSPOVIDONE, FERRIC OXIDE RED, HYDROXYPROPYL CELLULOSE, UNSPECIFIED, HYPROMELLOSE 2208 (100000 MPA.S), HYPROMELLOSE 2208 (15000 MPA.S), HYPROMELLOSE 2910 (5 MPA.S), MAGNESIUM STEARATE, MANNITOL, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL 400, POLYETHYLENE GLYCOL 6000, SILICON DIOXIDE, SODIUM LAURYL SULFATE, SODIUM STARCH GLYCOLATE TYPE A POTATO, STARCH, CORN |
| Chiesi USA, Inc. 1 product | ||
| 600 mg tabletNDC 10122-0901-12 | Corn-derived Titanium dioxide Propylene glycol |
Show 10 ingredientsCELLULOSE, MICROCRYSTALLINE, CROSPOVIDONE, HYDROXYPROPYL CELLULOSE (1600000 WAMW), HYPROMELLOSES, MAGNESIUM STEARATE, PROPYLENE GLYCOL, SODIUM STARCH GLYCOLATE TYPE A POTATO, STARCH, CORN, TALC, TITANIUM DIOXIDE |
| Golden State Medical Supply, Inc. 1 product | ||
| 600 mg extended-release tabletNDC 51407-0741-12 | Corn-derived Polyethylene glycol or polysorbate Sorbitol or mannitol |
Show 12 ingredientsFERRIC OXIDE RED, GLYCERYL BEHENATE/EICOSADIOATE, HYDROXYPROPYL CELLULOSE (110000 WAMW), HYPROMELLOSE 2208 (100 MPA.S), HYPROMELLOSE 2910 (10000 MPA.S), MAGNESIUM STEARATE, MANNITOL, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL 1000, SILICON DIOXIDE, SODIUM STARCH GLYCOLATE TYPE A POTATO, STARCH, CORN |
| NorthStar RxLLC 1 product | ||
| 600 mg extended-release tabletNDC 72603-0246-01 | Corn-derived Polyethylene glycol or polysorbate Sorbitol or mannitol |
Show 15 ingredientsCROSPOVIDONE, FERRIC OXIDE RED, HYDROXYPROPYL CELLULOSE, UNSPECIFIED, HYPROMELLOSE 2208 (100000 MPA.S), HYPROMELLOSE 2208 (15000 MPA.S), HYPROMELLOSE 2910 (5 MPA.S), MAGNESIUM STEARATE, MANNITOL, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL 400, POLYETHYLENE GLYCOL 6000, SILICON DIOXIDE, SODIUM LAURYL SULFATE, SODIUM STARCH GLYCOLATE TYPE A POTATO, STARCH, CORN |
| Rising Pharma Holdings, Inc. 1 product | ||
| 600 mg extended-release tabletNDC 64980-0206-12 | Corn-derived Titanium dioxide Polyethylene glycol or polysorbate Sorbitol or mannitol |
Show 14 ingredientsCROSPOVIDONE, FERRIC OXIDE YELLOW, HYDROXYPROPYL CELLULOSE (110000 WAMW), HYPROMELLOSE 2208 (15000 MPA.S), HYPROMELLOSE 2208 (200000 MPA.S), MAGNESIUM STEARATE, MANNITOL, MICROCRYSTALLINE CELLULOSE 101, POLYETHYLENE GLYCOL 400, SILICON DIOXIDE, SODIUM LAURYL SULFATE, SODIUM STARCH GLYCOLATE TYPE A POTATO, STARCH, CORN, TITANIUM DIOXIDE |
| Strides Pharma Science Limited 1 product | ||
| 600 mg extended-release tabletNDC 64380-0189-01 | Corn-derived Polyethylene glycol or polysorbate Sorbitol or mannitol |
Show 12 ingredientsFERRIC OXIDE RED, GLYCERYL BEHENATE/EICOSADIOATE, HYDROXYPROPYL CELLULOSE (110000 WAMW), HYPROMELLOSE 2208 (100 MPA.S), HYPROMELLOSE 2910 (10000 MPA.S), MAGNESIUM STEARATE, MANNITOL, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL 1000, SILICON DIOXIDE, SODIUM STARCH GLYCOLATE TYPE A POTATO, STARCH, CORN |
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.
Zileuton and corn-derived ingredients
Corn-derived: corn starch, maize or corn syrup; a concern with corn allergy. Every checked Zileuton product (6) lists corn-derived ingredients.
Lists corn-derived ingredients
- Camber: 600 mg extended-release tablet
- Chiesi: 600 mg tablet
- Golden State Medical Supply: 600 mg extended-release tablet
- NorthStar RxLLC: 600 mg extended-release tablet
- Rising: 600 mg extended-release tablet
- Strides Pharma Science: 600 mg extended-release tablet
Zileuton without titanium dioxide
Titanium dioxide: A white colorant some people choose to avoid. 2 of 6 checked products list titanium dioxide; 4 do not.
Does not list titanium dioxide
- Camber: 600 mg extended-release tablet
- Golden State Medical Supply: 600 mg extended-release tablet
- NorthStar RxLLC: 600 mg extended-release tablet
- Strides Pharma Science: 600 mg extended-release tablet
Lists titanium dioxide
- Chiesi: 600 mg tablet
- Rising: 600 mg extended-release tablet
Zileuton without propylene glycol
Propylene glycol: A solvent in liquids and capsules; a concern in kidney disease, for infants, and at high doses. 1 of 6 checked products list propylene glycol; 5 do not.
Does not list propylene glycol
- Camber: 600 mg extended-release tablet
- Golden State Medical Supply: 600 mg extended-release tablet
- NorthStar RxLLC: 600 mg extended-release tablet
- Rising: 600 mg extended-release tablet
- Strides Pharma Science: 600 mg extended-release tablet
Lists propylene glycol
- Chiesi: 600 mg tablet
Zileuton without polyethylene glycol or polysorbate
Polyethylene glycol or polysorbate: PEG, macrogol or polysorbate; a rare cause of allergic reactions. 5 of 6 checked products list polyethylene glycol or polysorbate; 1 does not.
Does not list polyethylene glycol or polysorbate
- Chiesi: 600 mg tablet
Lists polyethylene glycol or polysorbate
- Camber: 600 mg extended-release tablet
- Golden State Medical Supply: 600 mg extended-release tablet
- NorthStar RxLLC: 600 mg extended-release tablet
- Rising: 600 mg extended-release tablet
- Strides Pharma Science: 600 mg extended-release tablet
Zileuton without sorbitol or mannitol
Sorbitol or mannitol: sugar alcohols that can cause bloating or diarrhea in larger amounts. 5 of 6 checked products list sorbitol or mannitol; 1 does not.
Does not list sorbitol or mannitol
- Chiesi: 600 mg tablet
Lists sorbitol or mannitol
- Camber: 600 mg extended-release tablet
- Golden State Medical Supply: 600 mg extended-release tablet
- NorthStar RxLLC: 600 mg extended-release tablet
- Rising: 600 mg extended-release tablet
- Strides Pharma Science: 600 mg extended-release tablet
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 Zileuton inactive ingredients
Is Zileuton gluten-free?
Does Zileuton contain lactose?
Does Zileuton contain soy?
Is there a dye-free Zileuton?
Does Zileuton 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 Zileuton products in the FDA's current NDC directory (openFDA), as of October 6, 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 Zileuton guide