Aluminum Hydroxide inactive ingredients by manufacturer
Wondering whether your Aluminum Hydroxide 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 Aluminum Hydroxide 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 2 of the 4 current Aluminum Hydroxide products on the market today, from 4 companies listing it with the FDA, and lined them up side by side. 2 are still being read and will appear on a later visit.
Ask about your bottle
Is there something in your Aluminum Hydroxide? 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 Aluminum Hydroxide products list lactose, a gluten source, soy, dyes or gelatin?
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LactoseNo checked product
No checked Aluminum Hydroxide product lists lactose.
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Wheat or gluten sourceNo checked product
No checked Aluminum Hydroxide product lists a wheat or gluten source.
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SoyNo checked product
No checked Aluminum Hydroxide product lists soy.
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Synthetic dyesNo checked product
No checked Aluminum Hydroxide product lists synthetic dyes.
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GelatinNo checked product
No checked Aluminum Hydroxide product lists gelatin.
Also listed by some products: Corn 2 of 2 Propylene glycol 2 of 2 PEG or polysorbate 2 of 2
Find a version without it
Every current Aluminum Hydroxide product and what its label lists
| Product | Lists | Inactive ingredients on the label |
|---|---|---|
| Atlantic Biologicals Corp. 1 product | ||
| 320 mg/5 mL oral solutionNDC 17856-0091-03 | Still being read | Not read yet |
| Gentell LLC 1 product | ||
| 2 g/100 g ointment or gel topical creamNDC 61554-0318-11 | Corn-derived Propylene glycol Polyethylene glycol or polysorbate |
Show 18 ingredientsCALCIUM CARBONATE, CHOLECALCIFEROL, CITRIC ACID, ETHYLHEXYLGLYCERIN, GLYCERYL MONOSTEARATE, LANOLIN, MAGNESIUM HYDROXIDE, PEG-100 STEARATE, PETROLATUM, PHENOXYETHANOL, PROPYLENE GLYCOL, RETINYL PALMITATE, SODIUM CHLORIDE, SODIUM LAURETH SULFATE, STEARYL ALCOHOL, WATER, ZEA MAYS (CORN) OIL, ZINC CHLORIDE |
| Rugby Laboratories 1 product | ||
| 320 mg/5 mL oral solutionNDC 00536-0091-85 | Still being read | Not read yet |
| Twin Med LLC 1 product | ||
| 2 g/100 g ointment or gel topical creamNDC 55681-0031-04 | Corn-derived Propylene glycol Polyethylene glycol or polysorbate |
Show 18 ingredientsCALCIUM CARBONATE, CHOLECALCIFEROL, CITRIC ACID, ETHYLHEXYLGLYCERIN, GLYCERYL MONOSTEARATE, GLYCERYL STEARATE/PEG-100 STEARATE, LANOLIN, MAGNESIUM HYDROXIDE, PETROLATUM, PHENOXYETHANOL, PROPYLENE GLYCOL, RETINYL PALMITATE, SODIUM CHLORIDE, SODIUM LAURETH SULFATE, STEARYL ALCOHOL, WATER, ZEA MAYS (CORN) OIL, ZINC CHLORIDE |
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.
Aluminum Hydroxide and corn-derived ingredients
Corn-derived: corn starch, maize or corn syrup; a concern with corn allergy. Every checked Aluminum Hydroxide product (2) lists corn-derived ingredients.
Lists corn-derived ingredients
- Gentell: 2 g/100 g ointment or gel topical cream
- Twin Med: 2 g/100 g ointment or gel topical cream
Aluminum Hydroxide and propylene glycol
Propylene glycol: A solvent in liquids and capsules; a concern in kidney disease, for infants, and at high doses. Every checked Aluminum Hydroxide product (2) lists propylene glycol.
Lists propylene glycol
- Gentell: 2 g/100 g ointment or gel topical cream
- Twin Med: 2 g/100 g ointment or gel topical cream
Aluminum Hydroxide and polyethylene glycol or polysorbate
Polyethylene glycol or polysorbate: PEG, macrogol or polysorbate; a rare cause of allergic reactions. Every checked Aluminum Hydroxide product (2) lists polyethylene glycol or polysorbate.
Lists polyethylene glycol or polysorbate
- Gentell: 2 g/100 g ointment or gel topical cream
- Twin Med: 2 g/100 g ointment or gel topical cream
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 Aluminum Hydroxide inactive ingredients
Is Aluminum Hydroxide gluten-free?
Does Aluminum Hydroxide contain lactose?
Does Aluminum Hydroxide contain soy?
Is there a dye-free Aluminum Hydroxide?
Does Aluminum Hydroxide 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 Aluminum Hydroxide 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 Aluminum Hydroxide guide