Tobramycin inactive ingredients by manufacturer
Wondering whether your Tobramycin 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 Tobramycin 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 55 of the 66 current Tobramycin products on the market today, from 46 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. 6 labels have no inactive-ingredient list we could read, so those products cannot be compared.
Ask about your bottle
Is there something in your Tobramycin? 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 Tobramycin products list lactose, a gluten source, soy, dyes or gelatin?
-
LactoseNo checked product
No checked Tobramycin product lists lactose.
-
Wheat or gluten sourceNo checked product
No checked Tobramycin product lists a wheat or gluten source.
-
SoyNo checked product
No checked Tobramycin product lists soy.
-
Synthetic dyesNo checked product
No checked Tobramycin product lists synthetic dyes.
-
GelatinNo checked product
No checked Tobramycin product lists gelatin.
Also listed by some products: Sulfites 10 of 55
Find a version without it
Every current Tobramycin product and what its label lists
| Product | Lists | Inactive ingredients on the label |
|---|---|---|
| A-S Medication Solutions 2 products | ||
| 3 mg/mL eye dropsNDC 50090-2127-00 | None of these listed |
Show 7 ingredientsBORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, SODIUM SULFATE, SULFURIC ACID, TYLOXAPOL, WATER |
| 3 mg/mL eye dropsNDC 50090-4190-00 | None of these listed |
Show 8 ingredientsBENZALKONIUM CHLORIDE, BORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, SODIUM SULFATE ANHYDROUS, SULFURIC ACID, TYLOXAPOL, WATER |
| Advanced Rx Pharmacy of Tennessee, LLC 1 product | ||
| 3 mg/mL eye dropsNDC 80425-0341-01 | None of these listed |
Show 7 ingredientsBORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, SODIUM SULFATE, SULFURIC ACID, TYLOXAPOL, WATER |
| Alembic Pharmaceuticals Inc. 1 product | ||
| 3 mg/mL eye dropsNDC 62332-0518-05 | None of these listed |
Show 8 ingredientsBENZALKONIUM CHLORIDE, BORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, SODIUM SULFATE, SULFURIC ACID, TYLOXAPOL, WATER |
| Alembic Pharmaceuticals Limited 1 product | ||
| 3 mg/mL eye dropsNDC 46708-0518-05 | None of these listed |
Show 8 ingredientsBENZALKONIUM CHLORIDE, BORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, SODIUM SULFATE, SULFURIC ACID, TYLOXAPOL, WATER |
| American Health Packaging 1 product | ||
| 300 mg/5 mL inhalation solution (nebulizer)NDC 60687-0731-83 | None of these listed |
Show 5 ingredientsNITROGEN, SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER |
| Amneal Pharmaceuticals LLC 1 product | ||
| 300 mg/5 mL inhalation solution (nebulizer)NDC 65162-0914-46 | None of these listed |
Show 4 ingredientsSODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER |
| Ascend Laboratories, LLC 1 product | ||
| 300 mg/5 mL inhalation solution (nebulizer)NDC 67877-0678-70 | None of these listed |
Show 4 ingredientsSODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER |
| Asclemed USA, Inc. 2 products | ||
| 3 mg/mL eye dropsNDC 76420-0791-05 | Still being read | Not read yet |
| 3 mg/mL eye dropsNDC 76420-0092-05 | Still being read | Not read yet |
| Aurobindo Pharma Limited 1 product | ||
| 300 mg/5 mL inhalation solution (nebulizer)NDC 59651-0129-56 | None of these listed |
Show 4 ingredientsSODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER |
| Bausch & Lomb Incorporated 1 product | ||
| 3 mg/mL eye dropsNDC 24208-0290-05 | None of these listed |
Show 7 ingredientsBORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, SODIUM SULFATE, SULFURIC ACID, TYLOXAPOL, WATER |
| Baxter Healthcare Corporation 2 products | ||
| 40 mg/mL injectionNDC 36000-0242-01 | Sulfites |
Show 6 ingredientsEDETATE DISODIUM, PHENOL, SODIUM HYDROXIDE, SODIUM METABISULFITE, SULFURIC ACID, WATER |
| 40 mg/mL injectionNDC 36000-0244-25 | Sulfites |
Show 6 ingredientsEDETATE DISODIUM, PHENOL, SODIUM HYDROXIDE, SODIUM METABISULFITE, SULFURIC ACID, WATER |
| Belcher Pharmaceuticals, LLC 1 product | ||
| 3 mg/mL eye dropsNDC 62250-0110-01 | None of these listed |
Show 8 ingredientsBENZALKONIUM CHLORIDE, BORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, SODIUM SULFATE, SULFURIC ACID, TYLOXAPOL, WATER |
| Chiesi USA, Inc. 1 product | ||
| 300 mg/4 mL inhalation solution (nebulizer)NDC 10122-0820-04 | None of these listed |
Show 4 ingredientsSODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER |
| DirectRX 1 product | ||
| 3 mg/mL eye dropsNDC 61919-0642-05 | None of these listed |
Show 8 ingredientsBENZALKONIUM CHLORIDE, BORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, SODIUM SULFATE ANHYDROUS, SULFURIC ACID, TYLOXAPOL, WATER |
| Dr. Reddy's Laboratories Inc. 1 product | ||
| 300 mg/5 mL inhalerNDC 43598-0605-56 | None of these listed |
Show 4 ingredientsNitrogen, Sodium Chloride, Sodium Hydroxide, Sulfuric Acid |
| Eugia US LLC 1 product | ||
| 1.2 g/30 mL injectionNDC 55150-0470-06 | None of these listed |
Show 2 ingredientsSODIUM HYDROXIDE, SULFURIC ACID |
| Fosun Pharma USA Inc 1 product | ||
| 1.2 g/30 mL injectionNDC 72266-0163-06 | No inactive-ingredient list on the label | No list we could read |
| Fresenius Kabi USA, LLC 3 products | ||
| 10 mg/mL injectionNDC 63323-0305-02 | Sulfites |
Show 6 ingredientsEDETATE DISODIUM, PHENOL, SODIUM HYDROXIDE, SODIUM METABISULFITE, SULFURIC ACID, WATER |
| 40 mg/mL injectionNDC 63323-0306-02 | Sulfites |
Show 6 ingredientsEDETATE DISODIUM, PHENOL, SODIUM HYDROXIDE, SODIUM METABISULFITE, SULFURIC ACID, WATER |
| 1200 mg/30 mL injectionNDC 63323-0303-51 | None of these listed |
Show 1 ingredientWATER |
| Genericus, Inc. 1 product | ||
| 300 mg/5 mL inhalation solution (nebulizer)NDC 70644-0899-99 | None of these listed |
Show 3 ingredientsSodium Chloride, Sulfuric Acid, Water |
| Gland Pharma Limited 5 products | ||
| 3 mg/mL eye dropsNDC 68083-0374-01 | None of these listed |
Show 8 ingredientsBENZALKONIUM CHLORIDE, BORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, SODIUM SULFATE, SULFURIC ACID, TYLOXAPOL, WATER |
| 1.2 g/30 mL injectionNDC 68083-0312-06 | No inactive-ingredient list on the label | No list we could read |
| 10 mg/mL injectionNDC 68083-0253-25 | Sulfites |
Show 5 ingredientsEDETATE DISODIUM, SODIUM HYDROXIDE, SODIUM METABISULFITE, SULFURIC ACID, WATER |
| 40 mg/mL injectionNDC 68083-0241-01 | Sulfites |
Show 5 ingredientsEDETATE DISODIUM, SODIUM HYDROXIDE, SODIUM METABISULFITE, SULFURIC ACID, WATER |
| 40 mg/mL injectionNDC 68083-0254-25 | Sulfites |
Show 5 ingredientsEDETATE DISODIUM, SODIUM HYDROXIDE, SODIUM METABISULFITE, SULFURIC ACID, WATER |
| Hospira, Inc. 1 product | ||
| 40 mg/mL injectionNDC 00409-3578-01 | Sulfites |
Show 4 ingredientsEDETATE DISODIUM, SODIUM HYDROXIDE, SODIUM METABISULFITE, SULFURIC ACID |
| Jvet Pharmaceuticals Llc 1 product | ||
| 3 mg/mL eye dropsNDC 86211-0110-01 | None of these listed |
Show 8 ingredientsBENZALKONIUM CHLORIDE, BORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, SODIUM SULFATE, SULFURIC ACID, TYLOXAPOL, WATER |
| Lifestar Pharma LLC 2 products | ||
| 300 mg/4 mL inhalation solution (nebulizer)NDC 70756-0617-56 | None of these listed |
Show 4 ingredientsSODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER |
| 300 mg/5 mL inhalation solution (nebulizer)NDC 70756-0604-56 | None of these listed |
Show 4 ingredientsSODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER |
| Lupin Pharmaceuticals, Inc. 1 product | ||
| 300 mg/5 mL inhalation solution (nebulizer)NDC 68180-0962-56 | None of these listed |
Show 4 ingredientsSODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER |
| Micro Labs Limited 1 product | ||
| 300 mg/5 mL inhalerNDC 42571-0408-92 | None of these listed |
Show 4 ingredientsSODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER |
| Mylan Institutional LLC 2 products | ||
| 40 mg/mL injectionNDC 67457-0428-30 | Sulfites |
Show 6 ingredientsEDETATE DISODIUM, PHENOL, SODIUM BISULFITE, SODIUM HYDROXIDE, SULFURIC ACID, WATER |
| 40 mg/mL injectionNDC 67457-0473-22 | Sulfites |
Show 6 ingredientsEDETATE DISODIUM, PHENOL, SODIUM BISULFITE, SODIUM HYDROXIDE, SULFURIC ACID, WATER |
| Northstar Rx LLC 1 product | ||
| 1.2 g/30 mL injectionNDC 72603-0160-06 | No inactive-ingredient list on the label | No list we could read |
| NorthStar RxLLC 3 products | ||
| 300 mg/4 mL inhalation solution (nebulizer)NDC 72603-0630-56 | None of these listed |
Show 4 ingredientsSODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER |
| 300 mg/5 mL inhalation solution (nebulizer)NDC 72603-0430-56 | None of these listed |
Show 4 ingredientsSODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER |
| 300 mg/5 mL inhalerNDC 16714-0119-03 | None of these listed |
Show 4 ingredientsNitrogen, Sodium Chloride, Sodium Hydroxide, Sulfuric Acid |
| Novartis Pharmaceuticals Corporation 1 product | ||
| 3 mg/g eye ointmentNDC 00078-0813-01 | None of these listed |
Show 3 ingredientsCHLOROBUTANOL, MINERAL OIL, PETROLATUM |
| NuCare Pharmaceuticals,Inc. 2 products | ||
| 3 mg/mL eye dropsNDC 66267-0936-05 | None of these listed |
Show 7 ingredientsBORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, SODIUM SULFATE, SULFURIC ACID, TYLOXAPOL, WATER |
| 3 mg/mL eye dropsNDC 68071-2272-05 | Still being read | Not read yet |
| Pari Respiratory Equipment, Inc. 1 product | ||
| 300 mg/5 mL inhalation solution (nebulizer)NDC 24492-0850-56 | None of these listed |
Show 3 ingredientsSodium Chloride, Sulfuric Acid, Water |
| Prasco, LLC 1 product | ||
| 300 mg/4 mL inhalation solution (nebulizer)NDC 66993-0195-94 | None of these listed |
Show 4 ingredientsSODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER |
| Preferred Pharmaceuticals Inc. 2 products | ||
| 3 mg/mL eye dropsNDC 68788-4149-05 | None of these listed |
Show 7 ingredientsBORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, SODIUM SULFATE, SULFURIC ACID, TYLOXAPOL, WATER |
| 3 mg/mL eye dropsNDC 68788-7252-05 | None of these listed |
Show 8 ingredientsBENZALKONIUM CHLORIDE, BORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, SODIUM SULFATE ANHYDROUS, SULFURIC ACID, TYLOXAPOL, WATER |
| Proficient Rx LP 4 products | ||
| 3 mg/mL eye dropsNDC 63187-0024-05 | None of these listed |
Show 8 ingredientsBENZALKONIUM CHLORIDE, BORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, SODIUM SULFATE, SULFURIC ACID, TYLOXAPOL, WATER |
| 3 mg/mL eye dropsNDC 63187-0973-05 | None of these listed |
Show 8 ingredientsBENZALKONIUM CHLORIDE, BORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, SODIUM SULFATE, SULFURIC ACID, TYLOXAPOL, WATER |
| 3 mg/mL eye dropsNDC 63187-0902-02 | None of these listed |
Show 8 ingredientsBenzalkonium Chloride, Boric Acid, Sodium Chloride, Sodium Hydroxide, sodium Sulfate, Sulfuric Acid, Tyloxapol, WATER |
| 3 mg/mL eye dropsNDC 71205-0101-05 | Still being read | Not read yet |
| Remedyrepack Inc. 1 product | ||
| 3 mg/mL eye dropsNDC 70518-1370-00 | None of these listed |
Show 8 ingredientsBENZALKONIUM CHLORIDE, BORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, SODIUM SULFATE ANHYDROUS, SULFURIC ACID, TYLOXAPOL, WATER |
| Ritedose Pharmaceuticals, LLC 1 product | ||
| 300 mg/5 mL inhalation solution (nebulizer)NDC 76204-0029-56 | None of these listed |
Show 4 ingredientsSODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER |
| Sandoz Inc 1 product | ||
| 3 mg/mL eye dropsNDC 61314-0643-05 | None of these listed |
Show 8 ingredientsBENZALKONIUM CHLORIDE, BORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, SODIUM SULFATE, SULFURIC ACID, TYLOXAPOL, WATER |
| Slate Run Pharmaceuticals, LLC 1 product | ||
| 1200 mg/30 mL injectionNDC 70436-0110-36 | No inactive-ingredient list on the label | No list we could read |
| Somerset Therapeutics, LLC 1 product | ||
| 3 mg/mL eye dropsNDC 70069-0131-01 | None of these listed |
Show 8 ingredientsBENZALKONIUM CHLORIDE, BORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, SODIUM SULFATE ANHYDROUS, SULFURIC ACID, TYLOXAPOL, WATER |
| Sportpharm LLC 2 products | ||
| 3 mg/mL eye dropsNDC 85766-0025-05 | Still being read | Not read yet |
| 3 mg/mL eye dropsNDC 85766-0189-05 | None of these listed |
Show 8 ingredientsBENZALKONIUM CHLORIDE, BORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, SODIUM SULFATE ANHYDROUS, SULFURIC ACID, TYLOXAPOL, WATER |
| St. Mary's Medical Park Pharmacy 1 product | ||
| 3 mg/mL eye dropsNDC 60760-0583-05 | None of these listed |
Show 8 ingredientsBENZALKONIUM CHLORIDE, BORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, SODIUM SULFATE ANHYDROUS, SULFURIC ACID, TYLOXAPOL, WATER |
| Sun Pharmaceutical Industries, Inc. 1 product | ||
| 300 mg/5 mL inhalation solution (nebulizer)NDC 47335-0171-49 | None of these listed |
Show 5 ingredientsNITROGEN, SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER |
| Teva Pharmaceuticals USA, Inc. 1 product | ||
| 300 mg/5 mL inhalation solution (nebulizer)NDC 00093-4085-63 | None of these listed |
Show 4 ingredientsSODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER |
| Viatris Specialty LLC 2 products | ||
| 300 mg/5 mL inhalation solution (nebulizer)NDC 49502-0345-73 | None of these listed |
Show 4 ingredientsSODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER |
| 28 mg inhalerNDC 49502-0401-09 | None of these listed |
Show 3 ingredients1,2-DISTEAROYL-SN-GLYCERO-3-PHOSPHOCHOLINE, CALCIUM CHLORIDE, SULFURIC ACID |
| XGen Pharmaceuticals DJB, Inc. 1 product | ||
| 1.2 g/30 mL injectionNDC 39822-0412-01 | No inactive-ingredient list on the label | No list we could read |
| Xiromed LLC 1 product | ||
| 1.2 g/30 mL injectionNDC 70700-0173-22 | No inactive-ingredient list on the label | No list we could read |
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.
Tobramycin without sulfites
Sulfites: metabisulfite or bisulfite preservatives; a concern with sulfite sensitivity or asthma. 10 of 55 checked products list sulfites; 45 do not.
Does not list sulfites
- A-S Medication Solutions: 3 mg/mL eye drops (NDC 50090-2127-00), 3 mg/mL eye drops (NDC 50090-4190-00)
- Advanced Rx Pharmacy of Tennessee: 3 mg/mL eye drops
- Alembic Pharmaceuticals Inc.: 3 mg/mL eye drops
- Alembic Pharmaceuticals Limited: 3 mg/mL eye drops
- American Health Packaging: 300 mg/5 mL inhalation solution (nebulizer)
- Amneal: 300 mg/5 mL inhalation solution (nebulizer)
- Ascend: 300 mg/5 mL inhalation solution (nebulizer)
- Aurobindo: 300 mg/5 mL inhalation solution (nebulizer)
- Bausch & Lomb: 3 mg/mL eye drops
- Belcher: 3 mg/mL eye drops
- Chiesi: 300 mg/4 mL inhalation solution (nebulizer)
- DirectRX: 3 mg/mL eye drops
- Dr. Reddy's: 300 mg/5 mL inhaler
- Eugia: 1.2 g/30 mL injection
- Fresenius Kabi: 1200 mg/30 mL injection
- Genericus: 300 mg/5 mL inhalation solution (nebulizer)
- Gland: 3 mg/mL eye drops
- Jvet: 3 mg/mL eye drops
- Lifestar: 300 mg/4 mL inhalation solution (nebulizer), 300 mg/5 mL inhalation solution (nebulizer)
- Lupin: 300 mg/5 mL inhalation solution (nebulizer)
- Micro: 300 mg/5 mL inhaler
- NorthStar RxLLC: 300 mg/4 mL inhalation solution (nebulizer), 300 mg/5 mL inhalation solution (nebulizer), 300 mg/5 mL inhaler
- Novartis: 3 mg/g eye ointment
- NuCare: 3 mg/mL eye drops
- Pari Respiratory Equipment: 300 mg/5 mL inhalation solution (nebulizer)
- Prasco: 300 mg/4 mL inhalation solution (nebulizer)
- Preferred: 3 mg/mL eye drops (NDC 68788-4149-05), 3 mg/mL eye drops (NDC 68788-7252-05)
- Proficient Rx: 3 mg/mL eye drops (NDC 63187-0024-05), 3 mg/mL eye drops (NDC 63187-0973-05), 3 mg/mL eye drops (NDC 63187-0902-02)
- Remedyrepack: 3 mg/mL eye drops
- Ritedose: 300 mg/5 mL inhalation solution (nebulizer)
- Sandoz: 3 mg/mL eye drops
- Somerset Therapeutics: 3 mg/mL eye drops
- Sportpharm: 3 mg/mL eye drops
- St. Mary's Medical Park Pharmacy: 3 mg/mL eye drops
- Sun: 300 mg/5 mL inhalation solution (nebulizer)
- Teva: 300 mg/5 mL inhalation solution (nebulizer)
- Viatris Specialty: 300 mg/5 mL inhalation solution (nebulizer), 28 mg inhaler
Lists sulfites
- Baxter Healthcare: 40 mg/mL injection (NDC 36000-0242-01), 40 mg/mL injection (NDC 36000-0244-25)
- Fresenius Kabi: 10 mg/mL injection, 40 mg/mL injection
- Gland: 10 mg/mL injection, 40 mg/mL injection (NDC 68083-0241-01), 40 mg/mL injection (NDC 68083-0254-25)
- Hospira: 40 mg/mL injection
- Mylan Institutional: 40 mg/mL injection (NDC 67457-0428-30), 40 mg/mL injection (NDC 67457-0473-22)
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 Tobramycin inactive ingredients
Is Tobramycin gluten-free?
Does Tobramycin contain lactose?
Does Tobramycin contain soy?
Is there a dye-free Tobramycin?
Does Tobramycin 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 Tobramycin 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 Tobramycin guide