Flurbiprofen inactive ingredients by manufacturer
Wondering whether your Flurbiprofen 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 Flurbiprofen 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 7 of the 7 current Flurbiprofen products on the market today, from 7 companies listing it with the FDA, and lined them up side by side.
Ask about your bottle
Is there something in your Flurbiprofen? 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 Flurbiprofen products list lactose, a gluten source, soy, dyes or gelatin?
-
LactoseDiffers by manufacturer
3 of 7 checked products list lactose; 4 do not. See the products
-
Wheat or gluten sourceNo checked product
No checked Flurbiprofen product lists a wheat or gluten source.
-
SoyNo checked product
No checked Flurbiprofen product lists soy.
-
Synthetic dyesDiffers by manufacturer
3 of 7 checked products list synthetic dyes; 4 do not. See the products
-
GelatinNo checked product
No checked Flurbiprofen product lists gelatin.
Also listed by some products: Titanium dioxide 3 of 7 PEG or polysorbate 3 of 7
Find a version without it
Every current Flurbiprofen product and what its label lists
| Product | Lists | Inactive ingredients on the label |
|---|---|---|
| A-S Medication Solutions 1 product | ||
| 0.3 mg/mL eye dropsNDC 50090-3946-00 | None of these listed |
Show 10 ingredientsCITRIC ACID MONOHYDRATE, EDETATE DISODIUM, HYDROCHLORIC ACID, POLYVINYL ALCOHOL (100000 MW), POTASSIUM CHLORIDE, SODIUM CHLORIDE, SODIUM CITRATE, UNSPECIFIED FORM, SODIUM HYDROXIDE, THIMEROSAL, WATER |
| Amici Pharma, Inc. 1 product | ||
| 0.3 mg/mL eye dropsNDC 69292-0722-25 | None of these listed |
Show 10 ingredientsCITRIC ACID MONOHYDRATE, EDETATE DISODIUM, HYDROCHLORIC ACID, POLYVINYL ALCOHOL (100000 MW), POTASSIUM CHLORIDE, SODIUM CHLORIDE, SODIUM CITRATE, UNSPECIFIED FORM, SODIUM HYDROXIDE, THIMEROSAL, WATER |
| Bausch & Lomb Incorporated 1 product | ||
| 0.3 mg/mL eye dropsNDC 24208-0314-25 | None of these listed |
Show 10 ingredientsCITRIC ACID MONOHYDRATE, EDETATE DISODIUM, HYDROCHLORIC ACID, POLYVINYL ALCOHOL, UNSPECIFIED, POTASSIUM CHLORIDE, SODIUM CHLORIDE, SODIUM CITRATE, UNSPECIFIED FORM, SODIUM HYDROXIDE, THIMEROSAL, WATER |
| Genus Lifesciences 1 product | ||
| 100 mg tabletNDC 64950-0218-10 | Lactose Synthetic dyes Titanium dioxide Polyethylene glycol or polysorbate |
Show 11 ingredientsCROSCARMELLOSE SODIUM, FD&C BLUE NO. 1 ALUMINUM LAKE, HYPROMELLOSE 2910 (3 MPA.S), LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL 400, POLYETHYLENE GLYCOL 8000, POLYSORBATE 80, SILICON DIOXIDE, TITANIUM DIOXIDE |
| IPG Pharmaceuticals, Inc. 1 product | ||
| 100 mg tabletNDC 71085-0082-30 | Lactose Synthetic dyes Titanium dioxide Polyethylene glycol or polysorbate |
Show 11 ingredientsCROSCARMELLOSE SODIUM, FD&C BLUE NO. 1 ALUMINUM LAKE, HYPROMELLOSE 2910 (3 MPA.S), LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL 400, POLYETHYLENE GLYCOL 8000, POLYSORBATE 80, SILICON DIOXIDE, TITANIUM DIOXIDE |
| NuCare Pharmaceuticals,Inc. 1 product | ||
| 100 mg tabletNDC 68071-4436-04 | Lactose Synthetic dyes Titanium dioxide Polyethylene glycol or polysorbate |
Show 12 ingredientsCROSCARMELLOSE SODIUM, FD&C BLUE NO. 1, HYPROMELLOSE 2910 (3 MPA.S), HYPROMELLOSE 2910 (6 MPA.S), LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL 400, POLYETHYLENE GLYCOL 8000, POLYSORBATE 80, SILICON DIOXIDE, TITANIUM DIOXIDE |
| Proficient Rx LP 1 product | ||
| 0.3 mg/mL eye dropsNDC 63187-0937-25 | None of these listed |
Show 10 ingredientsCITRIC ACID MONOHYDRATE, EDETATE DISODIUM, HYDROCHLORIC ACID, POLYVINYL ALCOHOL, UNSPECIFIED, POTASSIUM CHLORIDE, SODIUM CHLORIDE, SODIUM CITRATE, UNSPECIFIED FORM, SODIUM HYDROXIDE, THIMEROSAL, 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.
Flurbiprofen without lactose
Lactose: milk sugar; a concern with lactose intolerance or a milk allergy. 3 of 7 checked products list lactose; 4 do not.
Does not list lactose
- A-S Medication Solutions: 0.3 mg/mL eye drops
- Amici: 0.3 mg/mL eye drops
- Bausch & Lomb: 0.3 mg/mL eye drops
- Proficient Rx: 0.3 mg/mL eye drops
Lists lactose
- Genus Lifesciences: 100 mg tablet
- IPG: 100 mg tablet
- NuCare: 100 mg tablet
Flurbiprofen without synthetic dyes
Synthetic dyes: FD&C or D&C colorants and their aluminum lakes. 3 of 7 checked products list synthetic dyes; 4 do not.
Does not list synthetic dyes
- A-S Medication Solutions: 0.3 mg/mL eye drops
- Amici: 0.3 mg/mL eye drops
- Bausch & Lomb: 0.3 mg/mL eye drops
- Proficient Rx: 0.3 mg/mL eye drops
Lists synthetic dyes
- Genus Lifesciences: 100 mg tablet
- IPG: 100 mg tablet
- NuCare: 100 mg tablet
Flurbiprofen without titanium dioxide
Titanium dioxide: A white colorant some people choose to avoid. 3 of 7 checked products list titanium dioxide; 4 do not.
Does not list titanium dioxide
- A-S Medication Solutions: 0.3 mg/mL eye drops
- Amici: 0.3 mg/mL eye drops
- Bausch & Lomb: 0.3 mg/mL eye drops
- Proficient Rx: 0.3 mg/mL eye drops
Lists titanium dioxide
- Genus Lifesciences: 100 mg tablet
- IPG: 100 mg tablet
- NuCare: 100 mg tablet
Flurbiprofen without polyethylene glycol or polysorbate
Polyethylene glycol or polysorbate: PEG, macrogol or polysorbate; a rare cause of allergic reactions. 3 of 7 checked products list polyethylene glycol or polysorbate; 4 do not.
Does not list polyethylene glycol or polysorbate
- A-S Medication Solutions: 0.3 mg/mL eye drops
- Amici: 0.3 mg/mL eye drops
- Bausch & Lomb: 0.3 mg/mL eye drops
- Proficient Rx: 0.3 mg/mL eye drops
Lists polyethylene glycol or polysorbate
- Genus Lifesciences: 100 mg tablet
- IPG: 100 mg tablet
- NuCare: 100 mg tablet
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 Flurbiprofen inactive ingredients
Is Flurbiprofen gluten-free?
Does Flurbiprofen contain lactose?
Does Flurbiprofen contain soy?
Is there a dye-free Flurbiprofen?
Does Flurbiprofen 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 Flurbiprofen 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 Flurbiprofen guide