Inactive ingredients by manufacturer

Imiquimod Topical inactive ingredients by manufacturer

Wondering whether your Imiquimod Topical 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 Imiquimod Topical 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 14 of the 14 current Imiquimod Topical 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 Imiquimod Topical? 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 Imiquimod Topical products list lactose, a gluten source, soy, dyes or gelatin?

  1. LactoseNo checked product

    No checked Imiquimod Topical product lists lactose.

  2. Wheat or gluten sourceNo checked product

    No checked Imiquimod Topical product lists a wheat or gluten source.

  3. SoyNo checked product

    No checked Imiquimod Topical product lists soy.

  4. Synthetic dyesNo checked product

    No checked Imiquimod Topical product lists synthetic dyes.

  5. GelatinNo checked product

    No checked Imiquimod Topical product lists gelatin.

Also listed by some products: Benzyl alcohol 14 of 14 PEG or polysorbate 14 of 14

Find a version without it

Every current Imiquimod Topical product and what its label lists

Hide products that list:

ProductListsInactive ingredients on the label
Anvi Pharmaceuticals Inc. 1 product
37.5 mg/g ointment or gel topical creamNDC 87519-0004-75 Benzyl alcohol Polyethylene glycol or polysorbate
Show 12 ingredients

BENZYL ALCOHOL, CETYL ALCOHOL, GLYCERIN, ISOSTEARIC ACID, METHYLPARABEN, PETROLATUM, POLYSORBATE 60, PROPYLPARABEN, SORBITAN MONOSTEARATE, STEARYL ALCOHOL, WATER, XANTHAN GUM
Bausch Health US, LLC 3 products
2.5 mg/g ointment or gel topical creamNDC 99207-0276-01 Benzyl alcohol Polyethylene glycol or polysorbate
Show 12 ingredients

BENZYL ALCOHOL, CETYL ALCOHOL, GLYCERIN, ISOSTEARIC ACID, METHYLPARABEN, PETROLATUM, POLYSORBATE 60, PROPYLPARABEN, SORBITAN MONOSTEARATE, STEARYL ALCOHOL, WATER, XANTHAN GUM
37.5 mg/g ointment or gel topical creamNDC 99207-0271-01 Benzyl alcohol Polyethylene glycol or polysorbate
Show 12 ingredients

BENZYL ALCOHOL, CETYL ALCOHOL, GLYCERIN, ISOSTEARIC ACID, METHYLPARABEN, PETROLATUM, POLYSORBATE 60, PROPYLPARABEN, SORBITAN MONOSTEARATE, STEARYL ALCOHOL, WATER, XANTHAN GUM
37.5 mg/g ointment or gel topical creamNDC 99207-0270-01 Benzyl alcohol Polyethylene glycol or polysorbate
Show 12 ingredients

BENZYL ALCOHOL, CETYL ALCOHOL, GLYCERIN, ISOSTEARIC ACID, METHYLPARABEN, PETROLATUM, POLYSORBATE 60, PROPYLPARABEN, SORBITAN MONOSTEARATE, STEARYL ALCOHOL, WATER, XANTHAN GUM
Bryant Ranch Prepack 3 products
12.5 mg/0.25 g ointment or gel topical creamNDC 71335-2725-01 Benzyl alcohol Polyethylene glycol or polysorbate
Show 13 ingredients

BENZYL ALCOHOL, CETYL ALCOHOL, GLYCERIN, METHYLPARABEN, OLEIC ACID, OLEYL ALCOHOL, PETROLATUM, POLYSORBATE 60, PROPYLPARABEN, SORBITAN MONOSTEARATE, STEARYL ALCOHOL, WATER, XANTHAN GUM
12.5 mg/0.25 g ointment or gel topical creamNDC 71335-3000-01 Benzyl alcohol Polyethylene glycol or polysorbate
Show 13 ingredients

BENZYL ALCOHOL, CETYL ALCOHOL, GLYCERIN, METHYLPARABEN, OLEIC ACID, OLEYL ALCOHOL, PETROLATUM, POLYSORBATE 60, PROPYLPARABEN, SORBITAN MONOSTEARATE, STEARYL ALCOHOL, WATER, XANTHAN GUM
12.5 mg/0.25 g ointment or gel topical creamNDC 72162-2332-02 Benzyl alcohol Polyethylene glycol or polysorbate
Show 13 ingredients

BENZYL ALCOHOL, CETYL ALCOHOL, GLYCERIN, METHYLPARABEN, OLEIC ACID, OLEYL ALCOHOL, PETROLATUM, POLYSORBATE 60, PROPYLPARABEN, SORBITAN MONOSTEARATE, STEARYL ALCOHOL, WATER, XANTHAN GUM
Direct Rx 1 product
12.5 mg/0.25 g ointment or gel topical creamNDC 72189-0084-24 Benzyl alcohol Polyethylene glycol or polysorbate
Show 13 ingredients

BENZYL ALCOHOL, CETYL ALCOHOL, GLYCERIN, METHYLPARABEN, OLEIC ACID, OLEYL ALCOHOL, PETROLATUM, POLYSORBATE 60, PROPYLPARABEN, SORBITAN MONOSTEARATE, STEARYL ALCOHOL, WATER, XANTHAN GUM
Glenmark Pharmaceuticals Inc., USA 1 product
50 mg/g ointment or gel topical creamNDC 68462-0536-70 Benzyl alcohol Polyethylene glycol or polysorbate
Show 12 ingredients

BENZYL ALCOHOL, CETYL ALCOHOL, GLYCERIN, ISOSTEARIC ACID, METHYLPARABEN, PETROLATUM, POLYSORBATE 60, PROPYLPARABEN, SORBITAN MONOSTEARATE, STEARYL ALCOHOL, WATER, XANTHAN GUM
Oceanside Pharmacueticals 1 product
37.5 mg/g ointment or gel topical creamNDC 68682-0272-75 Benzyl alcohol Polyethylene glycol or polysorbate
Show 12 ingredients

BENZYL ALCOHOL, CETYL ALCOHOL, GLYCERIN, ISOSTEARIC ACID, METHYLPARABEN, PETROLATUM, POLYSORBATE 60, PROPYLPARABEN, SORBITAN MONOSTEARATE, STEARYL ALCOHOL, WATER, XANTHAN GUM
Padagis Israel Pharmaceuticals Ltd 1 product
12.5 mg/0.25 g ointment or gel topical creamNDC 45802-0368-53 Benzyl alcohol Polyethylene glycol or polysorbate
Show 13 ingredients

BENZYL ALCOHOL, CETYL ALCOHOL, GLYCERIN, METHYLPARABEN, OLEIC ACID, OLEYL ALCOHOL, PETROLATUM, POLYSORBATE 60, PROPYLPARABEN, SORBITAN MONOSTEARATE, STEARYL ALCOHOL, WATER, XANTHAN GUM
Sun Pharmaceutical Industries, Inc. 2 products
37.5 mg/g ointment or gel topical creamNDC 51672-4174-06 Benzyl alcohol Polyethylene glycol or polysorbate
Show 12 ingredients

BENZYL ALCOHOL, CETYL ALCOHOL, GLYCERIN, ISOSTEARIC ACID, METHYLPARABEN, PETROLATUM, POLYSORBATE 60, PROPYLPARABEN, SORBITAN MONOSTEARATE, STEARYL ALCOHOL, WATER, XANTHAN GUM
50 mg/g ointment or gel topical creamNDC 51672-4145-06 Benzyl alcohol Polyethylene glycol or polysorbate
Show 12 ingredients

BENZYL ALCOHOL, CETYL ALCOHOL, GLYCERIN, ISOSTEARIC ACID, METHYLPARABEN, PETROLATUM, POLYSORBATE 60, PROPYLPARABEN, SORBITAN MONOSTEARATE, STEARYL ALCOHOL, WATER, XANTHAN GUM
Teva Pharmaceuticals USA, Inc. 1 product
37.5 mg/g ointment or gel topical creamNDC 00093-3133-31 Benzyl alcohol Polyethylene glycol or polysorbate
Show 12 ingredients

BENZYL ALCOHOL, CETYL ALCOHOL, GLYCERIN, ISOSTEARIC ACID, METHYLPARABEN, PETROLATUM, POLYSORBATE 60, PROPYLPARABEN, SORBITAN MONOSTEARATE, STEARYL ALCOHOL, WATER, XANTHAN GUM

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.

Imiquimod Topical and benzyl alcohol

Benzyl alcohol: A preservative, mostly in injections and liquids; not for newborns. Every checked Imiquimod Topical product (14) lists benzyl alcohol.

Lists benzyl alcohol

Imiquimod Topical and polyethylene glycol or polysorbate

Polyethylene glycol or polysorbate: PEG, macrogol or polysorbate; a rare cause of allergic reactions. Every checked Imiquimod Topical product (14) lists polyethylene glycol or polysorbate.

Lists polyethylene glycol or polysorbate

At the pharmacy counter

How to use this at the pharmacy counter

  1. 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.
  2. 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.
  3. 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.
  4. 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.
Ask Dr. Staiger which Imiquimod Topical product suits you →

Common questions about Imiquimod Topical inactive ingredients

Is Imiquimod Topical gluten-free?
This page cannot certify any Imiquimod Topical product gluten-free; it reports what each label declares. Of the 14 products checked, none lists a wheat, barley, rye or gluten ingredient, and none lists a starch without a stated source. If you have celiac disease, ask the manufacturer's medical information line for a written gluten statement for the lot you have.
Does Imiquimod Topical contain lactose?
No checked Imiquimod Topical product lists lactose on its label. People with a milk allergy or a strong intolerance often prefer a version that does not list it.
Does Imiquimod Topical contain soy?
No checked Imiquimod Topical product lists a soy ingredient (soybean oil or soy lecithin) on its label. Soy lecithin is the usual form and the amount is small, but people with a soy allergy often prefer a version that does not list it.
Is there a dye-free Imiquimod Topical?
No checked Imiquimod Topical product lists a synthetic dye (an FD&C or D&C colorant) on its label. Colorants often differ by strength within one company's line, so compare the lists above strength by strength.
Does Imiquimod Topical contain gelatin?
No checked Imiquimod Topical product lists gelatin on its label. Gelatin is usually bovine or porcine and the label rarely says which; for kosher, halal or vegetarian needs, ask the manufacturer.
Why do the inactive ingredients differ between manufacturers?
A generic must match the brand's active ingredient, strength, dose form and how it is absorbed; its fillers, binders, coatings and colorants are the manufacturer's own choice. That is why one Imiquimod Topical product can list lactose and a dye while another from a different company lists neither.
Can my pharmacy give me a specific manufacturer's version?
Often, if you ask before the prescription is filled: many pharmacies order from wholesalers that carry several companies' versions and can request a particular one. Some pharmacies buy a generic from one contracted source only, and a few insurance plans cover only certain NDCs, so ask the pharmacist to check. Give them the NDC from this page; the company name alone is often enough.
How current is this list?
The products are the ones in the FDA's current NDC directory as of October 6, 2026, and each inactive-ingredient list is the manufacturer's FDA label as our label sync last read it. Formulations change, so check the label on your own bottle and ask your pharmacist if a refill looks different.

Sources: the products are the finished Imiquimod Topical 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 Imiquimod Topical guide