Flurandrenolide Topical Inactive Ingredients by Manufacturer
Wondering whether your Flurandrenolide Topical has lactose, gluten, soy, a dye or gelatin in it?
- Lactose
- Gluten source
- Soy
- Dyes
- Gelatin
Same medicine, different fillers. The coatings, colors and fillers differ from one company to the next. This page shows what each Flurandrenolide Topical product's FDA label lists, so you can pick a version that leaves out what you avoid.
Answers from the FDA labels
Ask About the Inactive Ingredients in Your Flurandrenolide Topical
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
Look Up Your Flurandrenolide Topical by NDC, Company or Strength
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: the form, then the strength, then the company.
This company lists more than one. Match the imprint on your pill, or the NDC on your pharmacy label.
2 What do you want to check?
Nothing tapped? We check the five big ones.
- Listed on the labelthe company names it.
- Not listedthe label does not name it.
- Source unclearthe label names a starch or maltodextrin without saying what plant it came from.
- Still being readwe have not finished this label yet.
Pick your bottle to read its label, or tap an ingredient to see which Flurandrenolide Topical products leave it out.
Summary of all Flurandrenolide Topical products
The checker above looks at one bottle. This is every current Flurandrenolide Topical product at once: 4 FDA labels from 2 companies.
Which Flurandrenolide Topical Products List Lactose, a Gluten Source, Soy, Dyes or Gelatin?
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LactoseNo checked product
No checked Flurandrenolide Topical product lists lactose.
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Wheat or gluten sourceNo checked product
No checked Flurandrenolide Topical product lists a wheat or gluten source.
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SoyNo checked product
No checked Flurandrenolide Topical product lists soy.
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Synthetic dyesNo checked product
No checked Flurandrenolide Topical product lists synthetic dyes.
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GelatinNo checked product
No checked Flurandrenolide Topical product lists gelatin.
Also listed by some products: Benzyl alcohol 2 of 4 Propylene glycol 2 of 4
Details of all Flurandrenolide Topical products
Every current Flurandrenolide Topical product, grouped by strength and form. Open one to see each company's NDC, package sizes and full inactive-ingredient list.
Find a version without it
Every Current Flurandrenolide 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 size. Codes that differ only in the last part are the same product in different pack sizes and share one label, so any of them finds the right product here. Two bottles of the same medicine from different companies can have different inactive ingredients, which is why the pharmacy needs the number, not just the name.
Flurandrenolide Topical FLURANDRENOLIDE 4 mcg/cm2 ointment or gel topical cream 1 company
| Company | Lists | Inactive ingredients on the label |
|---|---|---|
| AlmirallNDC 16110-0587-24 Same product, other package sizes: 16110-0587-80 (bottle of 1,500 cm2s) | No inactive-ingredient list on the label | No list we could read |
Flurandrenolide Topical 0.5 mg/g ointment or gel topical cream 1 company, 2 products Propylene glycol 2
| Company | Lists | Inactive ingredients on the label |
|---|---|---|
| INA PharmaceuticsNDC 74157-0130-07 White | Propylene glycol | Show 8 ingredientsCETYL ALCOHOL, CITRIC ACID MONOHYDRATE, MINERAL OIL, POLYOXYL 40 STEARATE, PROPYLENE GLYCOL, SODIUM CITRATE, UNSPECIFIED FORM, STEARIC ACID, WATER |
| INA PharmaceuticsNDC 74157-0180-60 | Propylene glycol | Show 8 ingredientsCETYL ALCOHOL, CITRIC ACID MONOHYDRATE, MINERAL OIL, POLYOXYL 40 STEARATE, PROPYLENE GLYCOL, SODIUM CITRATE, UNSPECIFIED FORM, STEARIC ACID, WATER |
Flurandrenolide Topical 0.5 mg/mL ointment or gel topical cream 2 companies, 3 products Benzyl alcohol 2
| Company | Lists | Inactive ingredients on the label |
|---|---|---|
| Bryant Ranch PrepackNDC 63629-8657-01 | Benzyl alcohol | Show 9 ingredientsBENZYL ALCOHOL, CETYL ALCOHOL, GLYCERIN, GLYCERYL MONOSTEARATE, MENTHOL, UNSPECIFIED FORM, MINERAL OIL, POLYOXYL 40 STEARATE, STEARIC ACID, WATER |
| Bryant Ranch PrepackNDC 72162-1439-02 | Benzyl alcohol | Show 9 ingredientsBENZYL ALCOHOL, CETYL ALCOHOL, GLYCERIN, GLYCERYL MONOSTEARATE, MENTHOL, UNSPECIFIED FORM, MINERAL OIL, POLYOXYL 40 STEARATE, STEARIC ACID, WATER |
| Padagis IsraelNDC 45802-0928-03 | Still being read | Not read yet |
A product with none of these on its label may still contain them. The label shows only what the company listed, and it often does not say where a starch or a flavor comes from. Some companies here repackage or sell another company's product under their own name. Tap an NDC to open that product's page with its full label.
Flurandrenolide Topical Without Benzyl Alcohol
Benzyl alcohol: A preservative, mostly in injections and liquids; not for newborns. 2 of 4 checked products list benzyl alcohol; 2 do not.
Show which Flurandrenolide Topical products list benzyl alcohol and which do not, by product and company
Does Not List Benzyl Alcohol
- 0.5 mg/g ointment or gel topical cream: INA Pharmaceutics (2 products)
Lists Benzyl Alcohol
- 0.5 mg/mL ointment or gel topical cream: Bryant Ranch Prepack (2 products)
Flurandrenolide Topical Without Propylene Glycol
Propylene glycol: A solvent in liquids and capsules; a concern in kidney disease, for infants, and at high doses. 2 of 4 checked products list propylene glycol; 2 do not.
Show which Flurandrenolide Topical products list propylene glycol and which do not, by product and company
Does Not List Propylene Glycol
- 0.5 mg/mL ointment or gel topical cream: Bryant Ranch Prepack (2 products)
Lists Propylene Glycol
- 0.5 mg/g ointment or gel topical cream: INA Pharmaceutics (2 products)
At the pharmacy counter
How to Get the Version You Want at the Pharmacy
- 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 Flurandrenolide Topical Inactive Ingredients
Is Flurandrenolide Topical gluten-free?
Does Flurandrenolide Topical contain lactose?
Does Flurandrenolide Topical contain soy?
Is there a dye-free Flurandrenolide Topical?
Does Flurandrenolide Topical contain gelatin?
Why do the inactive ingredients differ between manufacturers?
What can a label not tell me?
Who decides what counts as a gluten source, a dye or soy on this page?
The NDC on my bottle ends differently from the one on this page. Is it the same product?
Can my pharmacy give me a specific manufacturer's version?
How current is this list?
Sources: the products are the finished Flurandrenolide 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 Flurandrenolide Topical guide