Ciclopirox Topical inactive ingredients by manufacturer
Wondering whether your Ciclopirox 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 Ciclopirox 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 33 of the 39 current Ciclopirox Topical products on the market today, from 14 companies listing it with the FDA, and lined them up side by side. 5 are still being read and will appear on a later visit. 1 label has no inactive-ingredient list we could read, so that product cannot be compared.
Ask about your bottle
Is there something in your Ciclopirox 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 Ciclopirox Topical products list lactose, a gluten source, soy, dyes or gelatin?
-
LactoseNo checked product
No checked Ciclopirox Topical product lists lactose.
-
Wheat or gluten sourceNo checked product
No checked Ciclopirox Topical product lists a wheat or gluten source.
-
SoyNo checked product
No checked Ciclopirox Topical product lists soy.
-
Synthetic dyesNo checked product
No checked Ciclopirox Topical product lists synthetic dyes.
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GelatinNo checked product
No checked Ciclopirox Topical product lists gelatin.
Also listed by some products: Benzyl alcohol 14 of 33 PEG or polysorbate 16 of 33
Find a version without it
Every current Ciclopirox Topical product and what its label lists
| Product | Lists | Inactive ingredients on the label |
|---|---|---|
| A-S Medication Solutions 1 product | ||
| 80 mg/mL topical solutionNDC 50090-6562-00 | None of these listed |
Show 2 ingredientsETHYL ACETATE, ISOPROPYL ALCOHOL |
| Acella Pharmaceuticals, LLC 1 product | ||
| 80 mg/mL topical solutionNDC 42192-0715-06 | None of these listed |
Show 2 ingredientsETHYL ACETATE, ISOPROPYL ALCOHOL |
| Actavis Pharma, Inc. 1 product | ||
| 10 mg/0.96 mL ointment or gel topical creamNDC 00591-2159-90 | None of these listed |
Show 5 ingredientsDISODIUM LAURETH SULFOSUCCINATE, LAURETH-2, SODIUM CHLORIDE, SODIUM LAURETH-2 SULFATE, WATER |
| Advanced Rx Pharmacy of Tennessee, LLC 1 product | ||
| 7.7 mg/g ointment or gel topical creamNDC 80425-0225-01 | No inactive-ingredient list on the label | No list we could read |
| Bryant Ranch Prepack 20 products | ||
| 7.7 mg/g ointment or gel topical creamNDC 63629-8625-01 | Benzyl alcohol Polyethylene glycol or polysorbate |
Show 10 ingredientsBENZYL ALCOHOL, CETYL ALCOHOL, LACTIC ACID, UNSPECIFIED FORM, LIGHT MINERAL OIL, MYRISTYL ALCOHOL, OCTYLDODECANOL, POLYSORBATE 60, SORBITAN MONOSTEARATE, STEARYL ALCOHOL, WATER |
| 7.7 mg/g ointment or gel topical creamNDC 63629-8626-01 | Benzyl alcohol Polyethylene glycol or polysorbate |
Show 10 ingredientsBENZYL ALCOHOL, CETYL ALCOHOL, LACTIC ACID, UNSPECIFIED FORM, LIGHT MINERAL OIL, MYRISTYL ALCOHOL, OCTYLDODECANOL, POLYSORBATE 60, SORBITAN MONOSTEARATE, STEARYL ALCOHOL, WATER |
| 7.7 mg/g ointment or gel topical creamNDC 63629-8624-01 | Benzyl alcohol Polyethylene glycol or polysorbate |
Show 10 ingredientsBENZYL ALCOHOL, CETYL ALCOHOL, LACTIC ACID, UNSPECIFIED FORM, LIGHT MINERAL OIL, MYRISTYL ALCOHOL, OCTYLDODECANOL, POLYSORBATE 60, SORBITAN MONOSTEARATE, STEARYL ALCOHOL, WATER |
| 7.7 mg/g ointment or gel topical creamNDC 71335-2865-01 | Benzyl alcohol Polyethylene glycol or polysorbate |
Show 10 ingredientsBENZYL ALCOHOL, CETYL ALCOHOL, LACTIC ACID, UNSPECIFIED FORM, LIGHT MINERAL OIL, MYRISTYL ALCOHOL, OCTYLDODECANOL, POLYSORBATE 60, SORBITAN MONOSTEARATE, STEARYL ALCOHOL, WATER |
| 7.7 mg/g ointment or gel topical creamNDC 72162-1397-02 | Benzyl alcohol Polyethylene glycol or polysorbate |
Show 10 ingredientsBENZYL ALCOHOL, CETYL ALCOHOL, LACTIC ACID, UNSPECIFIED FORM, LIGHT MINERAL OIL, MYRISTYL ALCOHOL, OCTYLDODECANOL, POLYSORBATE 60, SORBITAN MONOSTEARATE, STEARYL ALCOHOL, WATER |
| 7.7 mg/g ointment or gel topical creamNDC 63629-8622-01 | Still being read | Not read yet |
| 7.7 mg/g ointment or gel topical creamNDC 71335-2757-01 | Still being read | Not read yet |
| 7.7 mg/g ointment or gel topical creamNDC 72162-1126-01 | Polyethylene glycol or polysorbate |
Show 7 ingredientsCARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED), DOCUSATE SODIUM, ISOPROPYL ALCOHOL, OCTYLDODECANOL, PEG/PPG-18/18 DIMETHICONE, SODIUM HYDROXIDE, WATER |
| 7.7 mg/g ointment or gel topical creamNDC 63629-8621-01 | Still being read | Not read yet |
| 7.7 mg/g ointment or gel topical creamNDC 63629-8620-01 | Still being read | Not read yet |
| 80 mg/mL topical solutionNDC 63629-8623-01 | None of these listed |
Show 2 ingredientsETHYL ACETATE, ISOPROPYL ALCOHOL |
| 80 mg/mL topical solutionNDC 72162-2076-01 | None of these listed |
Show 2 ingredientsETHYL ACETATE, ISOPROPYL ALCOHOL |
| 80 mg/mL topical solutionNDC 72162-1321-02 | None of these listed |
Show 2 ingredientsETHYL ACETATE, ISOPROPYL ALCOHOL |
| 80 mg/mL topical solutionNDC 71335-2836-01 | None of these listed |
Show 3 ingredientsBUTYL ESTER OF METHYL VINYL ETHER/MALEIC ANHYDRIDE COPOLYMER (125000 MW), ETHYL ACETATE, ISOPROPYL ALCOHOL |
| 80 mg/mL topical solutionNDC 72162-2298-02 | None of these listed |
Show 3 ingredientsBUTYL ESTER OF METHYL VINYL ETHER/MALEIC ANHYDRIDE COPOLYMER (125000 MW), ETHYL ACETATE, ISOPROPYL ALCOHOL |
| 7.7 mg/100 mL topical suspensionNDC 63629-8627-01 | Benzyl alcohol Polyethylene glycol or polysorbate |
Show 10 ingredientsBENZYL ALCOHOL, CETYL ALCOHOL, LACTIC ACID, UNSPECIFIED FORM, LIGHT MINERAL OIL, MYRISTYL ALCOHOL, OCTYLDODECANOL, POLYSORBATE 60, SORBITAN MONOSTEARATE, STEARYL ALCOHOL, WATER |
| 7.7 mg/100 mL topical suspensionNDC 71335-2717-01 | Benzyl alcohol Polyethylene glycol or polysorbate |
Show 10 ingredientsBENZYL ALCOHOL, CETYL ALCOHOL, LACTIC ACID, UNSPECIFIED FORM, LIGHT MINERAL OIL, MYRISTYL ALCOHOL, OCTYLDODECANOL, POLYSORBATE 60, SORBITAN MONOSTEARATE, STEARYL ALCOHOL, WATER |
| 7.7 mg/100 mL topical suspensionNDC 71335-2915-01 | Benzyl alcohol Polyethylene glycol or polysorbate |
Show 10 ingredientsBENZYL ALCOHOL, CETYL ALCOHOL, LACTIC ACID, UNSPECIFIED FORM, LIGHT MINERAL OIL, MYRISTYL ALCOHOL, OCTYLDODECANOL, POLYSORBATE 60, SORBITAN MONOSTEARATE, STEARYL ALCOHOL, WATER |
| 7.7 mg/100 mL topical suspensionNDC 63629-2522-01 | Benzyl alcohol Polyethylene glycol or polysorbate |
Show 10 ingredientsBENZYL ALCOHOL, CETYL ALCOHOL, LACTIC ACID, UNSPECIFIED FORM, LIGHT MINERAL OIL, MYRISTYL ALCOHOL, OCTYLDODECANOL, POLYSORBATE 60, SORBITAN MONOSTEARATE, STEARYL ALCOHOL, WATER |
| 7.7 mg/100 mL topical suspensionNDC 72162-1406-03 | Still being read | Not read yet |
| Chartwell RX, LLC 1 product | ||
| 71.3 mg/mL topical solutionNDC 62135-0814-45 | None of these listed |
Show 3 ingredientsBUTYL ESTER OF METHYL VINYL ETHER/MALEIC ANHYDRIDE COPOLYMER (125000 MW), ETHYL ACETATE, ISOPROPYL ALCOHOL |
| Cosette Pharmaceuticals, Inc. 1 product | ||
| 7.7 mg/g ointment or gel topical creamNDC 00713-0638-15 | Benzyl alcohol Polyethylene glycol or polysorbate |
Show 10 ingredientsBENZYL ALCOHOL, CETYL ALCOHOL, LACTIC ACID, MINERAL OIL, MYRISTYL ALCOHOL, OCTYLDODECANOL, POLYSORBATE 60, SORBITAN MONOSTEARATE, STEARYL ALCOHOL, WATER |
| Encube Ethicals, Inc. 2 products | ||
| 1 g/100 mL ointment or gel topical creamNDC 21922-0105-52 | None of these listed |
Show 5 ingredientsDISODIUM LAURETH SULFOSUCCINATE, LAURETH-2, SODIUM CHLORIDE, SODIUM LAURETH-2 SULFATE, WATER |
| 80 mg/mL topical solutionNDC 21922-0053-51 | None of these listed |
Show 3 ingredientsBUTYL ESTER OF METHYL VINYL ETHER/MALEIC ANHYDRIDE COPOLYMER (125000 MW), ETHYL ACETATE, ISOPROPYL ALCOHOL |
| Glenmark Pharmaceuticals Inc., USA 2 products | ||
| 7.7 mg/g ointment or gel topical creamNDC 68462-0297-17 | Benzyl alcohol Polyethylene glycol or polysorbate |
Show 10 ingredientsBENZYL ALCOHOL, CETYL ALCOHOL, LACTIC ACID, UNSPECIFIED FORM, LIGHT MINERAL OIL, MYRISTYL ALCOHOL, OCTYLDODECANOL, POLYSORBATE 60, SORBITAN MONOSTEARATE, STEARYL ALCOHOL, WATER |
| 7.7 mg/g ointment or gel topical creamNDC 68462-0455-35 | None of these listed |
Show 6 ingredientsCARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED), ISOPROPYL ALCOHOL, MEDIUM-CHAIN TRIGLYCERIDES, SODIUM HYDROXIDE, SODIUM LAURYL SULFATE, WATER |
| Padagis US LLC 1 product | ||
| 7.7 mg/g ointment or gel topical creamNDC 00574-2061-01 | Polyethylene glycol or polysorbate |
Show 7 ingredientsCARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED), DOCUSATE SODIUM, ISOPROPYL ALCOHOL, OCTYLDODECANOL, PEG/PPG-18/18 DIMETHICONE, SODIUM HYDROXIDE, WATER |
| Padagis Israel Pharmaceuticals Ltd 4 products | ||
| 1 g/100 mL ointment or gel topical creamNDC 45802-0401-09 | None of these listed |
Show 5 ingredientsDISODIUM LAURETH SULFOSUCCINATE, LAURETH-2, SODIUM CHLORIDE, SODIUM LAURETH-3 SULFATE, WATER |
| 7.7 mg/g ointment or gel topical creamNDC 45802-0138-11 | Benzyl alcohol Polyethylene glycol or polysorbate |
Show 10 ingredientsBENZYL ALCOHOL, CETYL ALCOHOL, LACTIC ACID, UNSPECIFIED FORM, LIGHT MINERAL OIL, MYRISTYL ALCOHOL, OCTYLDODECANOL, POLYSORBATE 60, SORBITAN MONOSTEARATE, STEARYL ALCOHOL, WATER |
| 80 mg/mL topical solutionNDC 45802-0141-67 | None of these listed |
Show 2 ingredientsETHYL ACETATE, ISOPROPYL ALCOHOL |
| 7.7 mg/100 mL topical suspensionNDC 45802-0400-46 | Benzyl alcohol Polyethylene glycol or polysorbate |
Show 10 ingredientsBENZYL ALCOHOL, CETYL ALCOHOL, LACTIC ACID, UNSPECIFIED FORM, LIGHT MINERAL OIL, MYRISTYL ALCOHOL, OCTYLDODECANOL, POLYSORBATE 60, SORBITAN MONOSTEARATE, STEARYL ALCOHOL, WATER |
| Preferred Pharmaceuticals, Inc. 1 product | ||
| 80 mg/mL topical solutionNDC 68788-6797-06 | None of these listed |
Show 2 ingredientsETHYL ACETATE, ISOPROPYL ALCOHOL |
| Preferred Pharmaceuticals Inc. 1 product | ||
| 80 mg/mL topical solutionNDC 68788-8755-06 | None of these listed |
Show 3 ingredientsBUTYL ESTER OF METHYL VINYL ETHER/MALEIC ANHYDRIDE COPOLYMER (125000 MW), ETHYL ACETATE, ISOPROPYL ALCOHOL |
| Sun Pharmaceutical Industries, Inc. 2 products | ||
| 7.7 mg/g ointment or gel topical creamNDC 51672-1318-01 | Benzyl alcohol Polyethylene glycol or polysorbate |
Show 11 ingredientsBENZYL ALCOHOL, CETYL ALCOHOL, COCO DIETHANOLAMIDE, LACTIC ACID, UNSPECIFIED FORM, MINERAL OIL, MYRISTYL ALCOHOL, OCTYLDODECANOL, POLYSORBATE 60, SORBITAN MONOSTEARATE, STEARYL ALCOHOL, WATER |
| 10 mg/0.96 mL ointment or gel topical creamNDC 51672-1351-08 | None of these listed |
Show 5 ingredientsDISODIUM LAURETH SULFOSUCCINATE, LAURETH-2, SODIUM CHLORIDE, SODIUM LAURETH-3 SULFATE, WATER |
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.
Ciclopirox Topical without benzyl alcohol
Benzyl alcohol: A preservative, mostly in injections and liquids; not for newborns. 14 of 33 checked products list benzyl alcohol; 19 do not.
Does not list benzyl alcohol
- A-S Medication Solutions: 80 mg/mL topical solution
- Acella: 80 mg/mL topical solution
- Actavis: 10 mg/0.96 mL ointment or gel topical cream
- Bryant Ranch Prepack: 7.7 mg/g ointment or gel topical cream, 80 mg/mL topical solution (NDC 63629-8623-01), 80 mg/mL topical solution (NDC 72162-2076-01), 80 mg/mL topical solution (NDC 72162-1321-02), 80 mg/mL topical solution (NDC 71335-2836-01), 80 mg/mL topical solution (NDC 72162-2298-02)
- Chartwell RX: 71.3 mg/mL topical solution
- Encube Ethicals: 1 g/100 mL ointment or gel topical cream, 80 mg/mL topical solution
- Glenmark: 7.7 mg/g ointment or gel topical cream
- Padagis: 7.7 mg/g ointment or gel topical cream
- Padagis Israel: 1 g/100 mL ointment or gel topical cream, 80 mg/mL topical solution
- Preferred Pharmaceuticals, Inc.: 80 mg/mL topical solution
- Preferred Pharmaceuticals Inc.: 80 mg/mL topical solution
- Sun: 10 mg/0.96 mL ointment or gel topical cream
Lists benzyl alcohol
- Bryant Ranch Prepack: 7.7 mg/g ointment or gel topical cream (NDC 63629-8625-01), 7.7 mg/g ointment or gel topical cream (NDC 63629-8626-01), 7.7 mg/g ointment or gel topical cream (NDC 63629-8624-01), 7.7 mg/g ointment or gel topical cream (NDC 71335-2865-01), 7.7 mg/g ointment or gel topical cream (NDC 72162-1397-02), 7.7 mg/100 mL topical suspension (NDC 63629-8627-01), 7.7 mg/100 mL topical suspension (NDC 71335-2717-01), 7.7 mg/100 mL topical suspension (NDC 71335-2915-01), 7.7 mg/100 mL topical suspension (NDC 63629-2522-01)
- Cosette: 7.7 mg/g ointment or gel topical cream
- Glenmark: 7.7 mg/g ointment or gel topical cream
- Padagis Israel: 7.7 mg/g ointment or gel topical cream, 7.7 mg/100 mL topical suspension
- Sun: 7.7 mg/g ointment or gel topical cream
Ciclopirox Topical without polyethylene glycol or polysorbate
Polyethylene glycol or polysorbate: PEG, macrogol or polysorbate; a rare cause of allergic reactions. 16 of 33 checked products list polyethylene glycol or polysorbate; 17 do not.
Does not list polyethylene glycol or polysorbate
- A-S Medication Solutions: 80 mg/mL topical solution
- Acella: 80 mg/mL topical solution
- Actavis: 10 mg/0.96 mL ointment or gel topical cream
- Bryant Ranch Prepack: 80 mg/mL topical solution (NDC 63629-8623-01), 80 mg/mL topical solution (NDC 72162-2076-01), 80 mg/mL topical solution (NDC 72162-1321-02), 80 mg/mL topical solution (NDC 71335-2836-01), 80 mg/mL topical solution (NDC 72162-2298-02)
- Chartwell RX: 71.3 mg/mL topical solution
- Encube Ethicals: 1 g/100 mL ointment or gel topical cream, 80 mg/mL topical solution
- Glenmark: 7.7 mg/g ointment or gel topical cream
- Padagis Israel: 1 g/100 mL ointment or gel topical cream, 80 mg/mL topical solution
- Preferred Pharmaceuticals, Inc.: 80 mg/mL topical solution
- Preferred Pharmaceuticals Inc.: 80 mg/mL topical solution
- Sun: 10 mg/0.96 mL ointment or gel topical cream
Lists polyethylene glycol or polysorbate
- Bryant Ranch Prepack: 7.7 mg/g ointment or gel topical cream (NDC 63629-8625-01), 7.7 mg/g ointment or gel topical cream (NDC 63629-8626-01), 7.7 mg/g ointment or gel topical cream (NDC 63629-8624-01), 7.7 mg/g ointment or gel topical cream (NDC 71335-2865-01), 7.7 mg/g ointment or gel topical cream (NDC 72162-1397-02), 7.7 mg/g ointment or gel topical cream (NDC 72162-1126-01), 7.7 mg/100 mL topical suspension (NDC 63629-8627-01), 7.7 mg/100 mL topical suspension (NDC 71335-2717-01), 7.7 mg/100 mL topical suspension (NDC 71335-2915-01), 7.7 mg/100 mL topical suspension (NDC 63629-2522-01)
- Cosette: 7.7 mg/g ointment or gel topical cream
- Glenmark: 7.7 mg/g ointment or gel topical cream
- Padagis: 7.7 mg/g ointment or gel topical cream
- Padagis Israel: 7.7 mg/g ointment or gel topical cream, 7.7 mg/100 mL topical suspension
- Sun: 7.7 mg/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 Ciclopirox Topical inactive ingredients
Is Ciclopirox Topical gluten-free?
Does Ciclopirox Topical contain lactose?
Does Ciclopirox Topical contain soy?
Is there a dye-free Ciclopirox Topical?
Does Ciclopirox Topical 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 Ciclopirox 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 Ciclopirox Topical guide