Naftifine Topical inactive ingredients by manufacturer
Wondering whether your Naftifine 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 Naftifine 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 5 of the 5 current Naftifine Topical products on the market today, from 3 companies listing it with the FDA, and lined them up side by side.
Ask about your bottle
Is there something in your Naftifine 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.
Check your bottle
Let's take a closer look at your Naftifine Topical.
Pick your bottle and tap what you want to check. The answer comes from that product's own FDA label, which is already on this page.
1 Which bottle do you have?
Or tap your way to it, one step at a time:
2 What do you want to check?
Nothing tapped? We check the five big ones.
Pick your bottle to read its label, or tap an ingredient to see which Naftifine Topical products leave it out.
At a glance
Which Naftifine Topical products list lactose, a gluten source, soy, dyes or gelatin?
-
LactoseNo checked product
No checked Naftifine Topical product lists lactose.
-
Wheat or gluten sourceNo checked product
No checked Naftifine Topical product lists a wheat or gluten source.
-
SoyNo checked product
No checked Naftifine Topical product lists soy.
-
Synthetic dyesNo checked product
No checked Naftifine Topical product lists synthetic dyes.
-
GelatinNo checked product
No checked Naftifine Topical product lists gelatin.
Also listed by some products: Alcohol 3 of 5 Benzyl alcohol 5 of 5 Propylene glycol 3 of 5 PEG or polysorbate 5 of 5
Find a version without it
Every current Naftifine Topical product and what its label lists
Fastest way: search by NDC. It is printed on your bottle's pharmacy label. If it is not, call your pharmacy: they have it on record.
An NDC (National Drug Code) is the FDA's number for one exact product from one company in one package size, written like 60505-0121-01: the first part is the company, the middle the product and strength, the last the package. Two bottles of the same medicine with different NDCs can have different inactive ingredients, which is why the pharmacy needs the number, not just the name.
Naftifine Topical 10 mg/g ointment or gel topical cream 1 company Benzyl alcohol 1 Polyethylene glycol or polysorbate 1
| Company | Lists | Inactive ingredients on the label |
|---|---|---|
| SunNDC 51672-1362-01 | Benzyl alcohol Polyethylene glycol or polysorbate |
Show 10 ingredientsBENZYL ALCOHOL, CETYL ALCOHOL, CETYL ESTERS WAX, HYDROCHLORIC ACID, ISOPROPYL MYRISTATE, POLYSORBATE 60, SODIUM HYDROXIDE, SORBITAN MONOSTEARATE, STEARYL ALCOHOL, WATER |
Naftifine Topical 20 mg/g ointment or gel topical cream 2 companies Benzyl alcohol 2 Polyethylene glycol or polysorbate 2 Alcohol (ethanol) 1 Propylene glycol 1
| Company | Lists | Inactive ingredients on the label |
|---|---|---|
| SunNDC 51672-1368-02 | Benzyl alcohol Polyethylene glycol or polysorbate |
Show 10 ingredientsBENZYL ALCOHOL, CETYL ALCOHOL, CETYL ESTERS WAX, HYDROCHLORIC ACID, ISOPROPYL MYRISTATE, POLYSORBATE 60, SODIUM HYDROXIDE, SORBITAN MONOSTEARATE, STEARYL ALCOHOL, WATER |
| SunNDC 51672-1376-03 | Alcohol (ethanol) Benzyl alcohol Propylene glycol Polyethylene glycol or polysorbate |
Show 8 ingredientsALCOHOL, BENZYL ALCOHOL, EDETATE DISODIUM, HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%), POLYSORBATE 20, PROPYLENE GLYCOL, TROLAMINE, WATER |
Naftifine Topical 2 g/100 g ointment or gel topical cream 2 companies Alcohol (ethanol) 2 Benzyl alcohol 2 Propylene glycol 2 Polyethylene glycol or polysorbate 2
| Company | Lists | Inactive ingredients on the label |
|---|---|---|
| LegacyNDC 83107-0023-45 | Alcohol (ethanol) Benzyl alcohol Propylene glycol Polyethylene glycol or polysorbate |
Show 8 ingredientsALCOHOL, BENZYL ALCOHOL, EDETATE DISODIUM, HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%), POLYSORBATE 20, PROPYLENE GLYCOL, TROLAMINE, WATER |
| SebelaNDC 54766-0772-45 | Alcohol (ethanol) Benzyl alcohol Propylene glycol Polyethylene glycol or polysorbate |
Show 8 ingredientsALCOHOL, BENZYL ALCOHOL, EDETATE DISODIUM, HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%), POLYSORBATE 20, PROPYLENE GLYCOL, TROLAMINE, 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.
Naftifine Topical without alcohol (ethanol)
Alcohol (ethanol): mostly in liquids; a concern in alcohol recovery, for children, or with disulfiram or metronidazole. 3 of 5 checked products list alcohol (ethanol); 2 do not.
Show which Naftifine Topical products list alcohol (ethanol) and which do not, by product and company
Does not list alcohol (ethanol)
Lists alcohol (ethanol)
- 20 mg/g ointment or gel topical cream: Sun
- 2 g/100 g ointment or gel topical cream: Legacy, Sebela
Naftifine Topical and benzyl alcohol
Benzyl alcohol: A preservative, mostly in injections and liquids; not for newborns. Every checked Naftifine Topical product (5) lists benzyl alcohol.
Show which Naftifine Topical products list benzyl alcohol and which do not, by product and company
Lists benzyl alcohol
- 10 mg/g ointment or gel topical cream: Sun
- 20 mg/g ointment or gel topical cream: Sun, Sun
- 2 g/100 g ointment or gel topical cream: Legacy, Sebela
Naftifine Topical without propylene glycol
Propylene glycol: A solvent in liquids and capsules; a concern in kidney disease, for infants, and at high doses. 3 of 5 checked products list propylene glycol; 2 do not.
Show which Naftifine Topical products list propylene glycol and which do not, by product and company
Does not list propylene glycol
Lists propylene glycol
- 20 mg/g ointment or gel topical cream: Sun
- 2 g/100 g ointment or gel topical cream: Legacy, Sebela
Naftifine Topical and polyethylene glycol or polysorbate
Polyethylene glycol or polysorbate: PEG, macrogol or polysorbate; a rare cause of allergic reactions. Every checked Naftifine Topical product (5) lists polyethylene glycol or polysorbate.
Show which Naftifine Topical products list polyethylene glycol or polysorbate and which do not, by product and company
Lists polyethylene glycol or polysorbate
- 10 mg/g ointment or gel topical cream: Sun
- 20 mg/g ointment or gel topical cream: Sun, Sun
- 2 g/100 g ointment or gel topical cream: Legacy, Sebela
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 Naftifine Topical inactive ingredients
Is Naftifine Topical gluten-free?
Does Naftifine Topical contain lactose?
Does Naftifine Topical contain soy?
Is there a dye-free Naftifine Topical?
Does Naftifine Topical contain gelatin?
Why do the inactive ingredients differ between manufacturers?
Who decides what counts as a gluten source, a dye or soy on this page?
Can my pharmacy give me a specific manufacturer's version?
How current is this list?
Sources: the products are the finished Naftifine 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 Naftifine Topical guide