Acetylcysteine inactive ingredients by manufacturer
Wondering whether your Acetylcysteine 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 Acetylcysteine 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 24 of the 30 current Acetylcysteine products on the market today, from 15 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. 1 label has no inactive-ingredient list we could read, so that product cannot be compared.
Ask about your bottle
Is there something in your Acetylcysteine? 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 Acetylcysteine products list lactose, a gluten source, soy, dyes or gelatin?
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LactoseNo checked product
No checked Acetylcysteine product lists lactose.
-
Wheat or gluten sourceNo checked product
No checked Acetylcysteine product lists a wheat or gluten source.
-
SoyNo checked product
No checked Acetylcysteine product lists soy.
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Synthetic dyesNo checked product
No checked Acetylcysteine product lists synthetic dyes.
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GelatinNo checked product
No checked Acetylcysteine product lists gelatin.
Find a version without it
Every current Acetylcysteine product and what its label lists
| Product | Lists | Inactive ingredients on the label |
|---|---|---|
| American Regent, Inc. 4 products | ||
| 100 mg/mL inhalerNDC 00517-7504-25 | None of these listed |
Show 2 ingredientsEDETATE DISODIUM, WATER |
| 100 mg/mL inhalerNDC 00517-7510-03 | None of these listed |
Show 2 ingredientsEDETATE DISODIUM, WATER |
| 200 mg/mL inhalerNDC 00517-7610-03 | Still being read | Not read yet |
| 200 mg/mL inhalerNDC 00517-7604-25 | None of these listed |
Show 2 ingredientsEDETATE DISODIUM, WATER |
| Cameron Pharmaceuticals 2 products | ||
| 100 mg/mL inhalation solution (nebulizer)NDC 42494-0435-25 | None of these listed |
Show 2 ingredientsEDETATE DISODIUM, Water |
| 200 mg/mL inhalation solution (nebulizer)NDC 42494-0436-25 | None of these listed |
Show 2 ingredientsEDETATE DISODIUM, Water |
| Cardinal Health 107, LLC 2 products | ||
| 100 mg/mL inhalerNDC 55154-5730-05 | None of these listed |
Show 2 ingredientsEDETATE DISODIUM, WATER |
| 200 mg/mL inhalerNDC 55154-5731-05 | Still being read | Not read yet |
| Cumberland Pharmaceuticals Inc. 1 product | ||
| 200 mg/mL injectionNDC 66220-0207-30 | Still being read | Not read yet |
| Eugia US LLC 1 product | ||
| 6 g/30 mL injectionNDC 55150-0259-30 | None of these listed |
Show 3 ingredientsEDETATE DISODIUM, SODIUM HYDROXIDE, WATER |
| Fresenius Kabi USA, LLC 7 products | ||
| 100 mg/mL inhalation solution (nebulizer)NDC 63323-0695-04 | None of these listed |
Show 3 ingredientsEDETATE DISODIUM, HYDROCHLORIC ACID, SODIUM HYDROXIDE |
| 100 mg/mL inhalation solution (nebulizer)NDC 63323-0691-30 | None of these listed |
Show 3 ingredientsEDETATE DISODIUM, HYDROCHLORIC ACID, SODIUM HYDROXIDE |
| 100 mg/mL inhalation solution (nebulizer)NDC 63323-0693-10 | None of these listed |
Show 3 ingredientsEDETATE DISODIUM, HYDROCHLORIC ACID, SODIUM HYDROXIDE |
| 200 mg/mL inhalation solution (nebulizer)NDC 63323-0694-04 | None of these listed |
Show 3 ingredientsEDETATE DISODIUM, HYDROCHLORIC ACID, SODIUM HYDROXIDE |
| 200 mg/mL inhalation solution (nebulizer)NDC 63323-0692-10 | None of these listed |
Show 3 ingredientsEDETATE DISODIUM, HYDROCHLORIC ACID, SODIUM HYDROXIDE |
| 200 mg/mL inhalation solution (nebulizer)NDC 63323-0690-30 | None of these listed |
Show 3 ingredientsEDETATE DISODIUM, HYDROCHLORIC ACID, SODIUM HYDROXIDE |
| 200 mg/mL injectionNDC 63323-0963-30 | None of these listed |
Show 3 ingredientsEDETATE DISODIUM, SODIUM HYDROXIDE, WATER |
| Glenmark Pharmaceuticals Inc., USA 1 product | ||
| 200 mg/mL injectionNDC 68462-0946-12 | None of these listed |
Show 3 ingredientsedetate disodium, Sodium Hydroxide, Water |
| Hikma Pharmaceuticals USA Inc. 1 product | ||
| 200 mg/mL injectionNDC 00143-9433-04 | No inactive-ingredient list on the label | No list we could read |
| Hospira, Inc. 2 products | ||
| 100 mg/mL inhalation solution (nebulizer)NDC 00409-3307-03 | None of these listed |
Show 3 ingredientsEDETATE DISODIUM, HYDROCHLORIC ACID, SODIUM HYDROXIDE |
| 200 mg/mL inhalation solution (nebulizer)NDC 00409-3308-03 | None of these listed |
Show 3 ingredientsEDETATE DISODIUM, HYDROCHLORIC ACID, SODIUM HYDROXIDE |
| Indoco Remedies Limited 1 product | ||
| 200 mg/mL injectionNDC 14445-0412-04 | None of these listed |
Show 3 ingredientsEDETATE DISODIUM, SODIUM HYDROXIDE, WATER |
| Onesource Specialty Pharma Limited 1 product | ||
| 200 mg/mL injectionNDC 83270-0001-04 | None of these listed |
Show 3 ingredientsEDETATE DISODIUM, SODIUM HYDROXIDE, WATER |
| Padagis US LLC 1 product | ||
| 200 mg/mL injectionNDC 00574-0805-30 | None of these listed |
Show 2 ingredientsSODIUM HYDROXIDE, WATER |
| Sagent Pharmaceuticals 1 product | ||
| 200 mg/mL injectionNDC 25021-0812-30 | Still being read | Not read yet |
| Somerset Therapeutics, LLC 4 products | ||
| 100 mg/mL inhalation solution (nebulizer)NDC 70069-0018-25 | None of these listed |
Show 3 ingredientsEDETATE DISODIUM, SODIUM HYDROXIDE, WATER |
| 200 mg/mL inhalation solution (nebulizer)NDC 70069-0020-03 | None of these listed |
Show 3 ingredientsEDETATE DISODIUM, SODIUM HYDROXIDE, WATER |
| 200 mg/mL inhalation solution (nebulizer)NDC 70069-0019-25 | None of these listed |
Show 3 ingredientsEDETATE DISODIUM, SODIUM HYDROXIDE, WATER |
| 200 mg/mL injectionNDC 70069-0788-04 | None of these listed |
Show 3 ingredientsNITROGEN, SODIUM HYDROXIDE, WATER |
| Xellia Pharmaceuticals USA LLC 1 product | ||
| 200 mg/mL injectionNDC 70594-0111-02 | Still being read | Not read yet |
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 Acetylcysteine inactive ingredients
Is Acetylcysteine gluten-free?
Does Acetylcysteine contain lactose?
Does Acetylcysteine contain soy?
Is there a dye-free Acetylcysteine?
Does Acetylcysteine 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 Acetylcysteine 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 Acetylcysteine guide