Gentamicin Ophthalmic inactive ingredients by manufacturer
Wondering whether your Gentamicin Ophthalmic 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 Gentamicin Ophthalmic 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 16 current Gentamicin Ophthalmic products on the market today, from 10 companies listing it with the FDA, and lined them up side by side. 2 are still being read and will appear on a later visit.
Ask about your bottle
Is there something in your Gentamicin Ophthalmic? 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 Gentamicin Ophthalmic products list lactose, a gluten source, soy, dyes or gelatin?
-
LactoseNo checked product
No checked Gentamicin Ophthalmic product lists lactose.
-
Wheat or gluten sourceNo checked product
No checked Gentamicin Ophthalmic product lists a wheat or gluten source.
-
SoyNo checked product
No checked Gentamicin Ophthalmic product lists soy.
-
Synthetic dyesNo checked product
No checked Gentamicin Ophthalmic product lists synthetic dyes.
-
GelatinNo checked product
No checked Gentamicin Ophthalmic product lists gelatin.
Find a version without it
Every current Gentamicin Ophthalmic product and what its label lists
| Product | Lists | Inactive ingredients on the label |
|---|---|---|
| A-S Medication Solutions 1 product | ||
| 3 mg/mL eye dropsNDC 50090-0569-00 | Still being read | Not read yet |
| Asclemed USA, Inc. 2 products | ||
| 3 mg/mL eye dropsNDC 76420-0137-05 | None of these listed |
Show 7 ingredientsBENZALKONIUM CHLORIDE, HYDROCHLORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, SODIUM PHOSPHATE, TYLOXAPOL, WATER |
| 3 mg/mL eye dropsNDC 76420-0254-05 | None of these listed |
Show 7 ingredientsBENZALKONIUM CHLORIDE, HYDROCHLORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, SODIUM PHOSPHATE, DIBASIC, UNSPECIFIED FORM, SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORM, WATER |
| Bausch & Lomb Incorporated 1 product | ||
| 3 mg/mL eye dropsNDC 24208-0580-60 | None of these listed |
Show 7 ingredientsBENZALKONIUM CHLORIDE, HYDROCHLORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, SODIUM PHOSPHATE, DIBASIC, UNSPECIFIED FORM, SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORM, WATER |
| Direct Rx 1 product | ||
| 3 mg/mL eye dropsNDC 61919-0106-05 | None of these listed |
Show 8 ingredientsBENZALKONIUM CHLORIDE, EDETATE DISODIUM, HYDROCHLORIC ACID, POLYVINYL ALCOHOL, SODIUM CHLORIDE, SODIUM HYDROXIDE, SODIUM PHOSPHATE, DIBASIC, WATER |
| Direct_Rx 1 product | ||
| 3 mg/mL eye dropsNDC 72189-0359-05 | None of these listed |
Show 7 ingredientsBENZALKONIUM CHLORIDE, HYDROCHLORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, SODIUM PHOSPHATE, DIBASIC, UNSPECIFIED FORM, SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORM, WATER |
| NuCare Pharmaceuticals,Inc. 3 products | ||
| 3 mg/mL eye dropsNDC 68071-4775-05 | Still being read | Not read yet |
| 3 mg/mL eye dropsNDC 68071-3554-05 | None of these listed |
Show 7 ingredientsBENZALKONIUM CHLORIDE, HYDROCHLORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, SODIUM PHOSPHATE, DIBASIC, UNSPECIFIED FORM, SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORM, WATER |
| 3 mg/mL eye dropsNDC 68071-4827-05 | None of these listed |
Show 8 ingredientsBENZALKONIUM CHLORIDE, EDETATE DISODIUM, HYDROCHLORIC ACID, POLYVINYL ALCOHOL, UNSPECIFIED, SODIUM CHLORIDE, SODIUM HYDROXIDE, SODIUM PHOSPHATE, DIBASIC, WATER |
| NuCare Pharmaceuticals, Inc. 1 product | ||
| 3 mg/mL eye dropsNDC 66267-0971-05 | None of these listed |
Show 4 ingredientsBENZALKONIUM CHLORIDE, SODIUM CHLORIDE, SODIUM PHOSPHATE, DIBASIC, ANHYDROUS, SODIUM PHOSPHATE, MONOBASIC |
| Preferred Pharmaceuticals Inc. 1 product | ||
| 3 mg/mL eye dropsNDC 68788-8592-05 | None of these listed |
Show 7 ingredientsBENZALKONIUM CHLORIDE, HYDROCHLORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, SODIUM PHOSPHATE, DIBASIC, UNSPECIFIED FORM, SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORM, WATER |
| Proficient Rx LP 4 products | ||
| 3 mg/mL eye dropsNDC 71205-0333-05 | None of these listed |
Show 7 ingredientsBENZALKONIUM CHLORIDE, HYDROCHLORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, SODIUM PHOSPHATE, TYLOXAPOL, WATER |
| 3 mg/mL eye dropsNDC 63187-0764-05 | None of these listed |
Show 4 ingredientsBenzalkonium Chloride, Sodium Chloride, Sodium Phosphate, Dibasic, Anhydrous, SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORM |
| 3 mg/mL eye dropsNDC 63187-0560-05 | None of these listed |
Show 7 ingredientsBENZALKONIUM CHLORIDE, HYDROCHLORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, SODIUM PHOSPHATE, DIBASIC, UNSPECIFIED FORM, SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORM, WATER |
| 3 mg/g eye ointmentNDC 63187-0873-35 | None of these listed |
Show 4 ingredientsMethylparaben, Mineral Oil, Petrolatum, Propylparaben |
| Sandoz Inc 1 product | ||
| 3 mg/mL eye dropsNDC 61314-0633-05 | None of these listed |
Show 7 ingredientsBENZALKONIUM CHLORIDE, HYDROCHLORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, SODIUM PHOSPHATE, DIBASIC, ANHYDROUS, TYLOXAPOL, 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.
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 Gentamicin Ophthalmic inactive ingredients
Is Gentamicin Ophthalmic gluten-free?
Does Gentamicin Ophthalmic contain lactose?
Does Gentamicin Ophthalmic contain soy?
Is there a dye-free Gentamicin Ophthalmic?
Does Gentamicin Ophthalmic 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 Gentamicin Ophthalmic 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 Gentamicin Ophthalmic guide