Inactive ingredients by manufacturer

Ipratropium inactive ingredients by manufacturer

Wondering whether your Ipratropium 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 Ipratropium 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 29 of the 35 current Ipratropium products on the market today, from 24 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 Ipratropium? 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 Ipratropium products list lactose, a gluten source, soy, dyes or gelatin?

  1. LactoseNo checked product

    No checked Ipratropium product lists lactose.

  2. Wheat or gluten sourceNo checked product

    No checked Ipratropium product lists a wheat or gluten source.

  3. SoyNo checked product

    No checked Ipratropium product lists soy.

  4. Synthetic dyesNo checked product

    No checked Ipratropium product lists synthetic dyes.

  5. GelatinNo checked product

    No checked Ipratropium product lists gelatin.

Also listed by some products: Alcohol 1 of 29

Find a version without it

Every current Ipratropium product and what its label lists

Hide products that list:

ProductListsInactive ingredients on the label
A-S Medication Solutions 3 products
0.5 mg/2.5 mL inhalation solution (nebulizer)NDC 50090-6373-00 Still being read Not read yet
0.5 mg/2.5 mL inhalation solution (nebulizer)NDC 50090-0668-00 None of these listed
Show 3 ingredients

HYDROCHLORIC ACID, SODIUM CHLORIDE, WATER
42 mcg nasal sprayNDC 50090-5968-00 None of these listed
Show 6 ingredients

AQUA, BENZALKONIUM CHLORIDE, EDETATE DISODIUM, HYDROCHLORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE
Advagen Pharma Ltd 2 products
21 mcg nasal sprayNDC 72888-0149-38 None of these listed
Show 4 ingredients

BENZALKONIUM CHLORIDE, EDETATE DISODIUM, SODIUM CHLORIDE, WATER
42 mcg nasal sprayNDC 72888-0148-37 None of these listed
Show 6 ingredients

BENZALKONIUM CHLORIDE, EDETATE DISODIUM, HYDROCHLORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER
American Health Packaging 1 product
0.5 mg/2.5 mL inhalation solution (nebulizer)NDC 60687-0394-83 None of these listed
Show 3 ingredients

HYDROCHLORIC ACID, SODIUM CHLORIDE, WATER
Amneal Pharmaceuticals NY LLC 2 products
21 mcg nasal sprayNDC 69238-2016-03 None of these listed
Show 6 ingredients

BENZALKONIUM CHLORIDE, EDETATE DISODIUM, HYDROCHLORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER
42 mcg nasal sprayNDC 69238-2017-02 None of these listed
Show 6 ingredients

BENZALKONIUM CHLORIDE, EDETATE DISODIUM, HYDROCHLORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER
Apotex Corp. 2 products
21 mcg nasal sprayNDC 60505-0826-01 None of these listed
Show 6 ingredients

BENZALKONIUM CHLORIDE, EDETATE DISODIUM, HYDROCHLORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER
42 mcg nasal sprayNDC 60505-0827-01 None of these listed
Show 6 ingredients

BENZALKONIUM CHLORIDE, EDETATE DISODIUM, HYDROCHLORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER
Armstrong Pharmaceuticals, Inc. 1 product
17 mcg inhalerNDC 17270-0401-00 Alcohol (ethanol)
Show 4 ingredients

1,1,1,2-TETRACHLOROETHANE, ANHYDROUS CITRIC ACID, DEHYDRATED ALCOHOL, WATER
Aurobindo Pharma Limited 1 product
0.5 mg/2.5 mL inhalation solution (nebulizer)NDC 65862-0905-03 None of these listed
Show 3 ingredients

HYDROCHLORIC ACID, SODIUM CHLORIDE, WATER
Bausch & Lomb Incorporated 2 products
21 mcg nasal sprayNDC 24208-0398-30 None of these listed
Show 6 ingredients

BENZALKONIUM CHLORIDE, EDETATE DISODIUM, HYDROCHLORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER
42 mcg nasal sprayNDC 24208-0399-15 Still being read Not read yet
Boehringer Ingelheim Pharmaceuticals, Inc. 1 product
17 mcg inhalerNDC 00597-0087-17 No inactive-ingredient list on the label No list we could read
Bryant Ranch Prepack 2 products
21 mcg nasal sprayNDC 72162-2143-03 None of these listed
Show 7 ingredients

BENZALKONIUM CHLORIDE, EDETATE CALCIUM DISODIUM, HYDROCHLORIC ACID, HYDROXYETHYL CELLULOSE (140 MPA.S AT 5%), SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER
42 mcg nasal sprayNDC 72162-2144-02 None of these listed
Show 7 ingredients

BENZALKONIUM CHLORIDE, EDETATE CALCIUM DISODIUM, HYDROCHLORIC ACID, HYDROXYETHYL CELLULOSE (140 MPA.S AT 5%), SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER
Cardinal Health 107, LLC 2 products
0.5 mg/2.5 mL inhalation solution (nebulizer)NDC 55154-4411-05 None of these listed
Show 3 ingredients

HYDROCHLORIC ACID, SODIUM CHLORIDE, WATER
0.5 mg/2.5 mL inhalation solution (nebulizer)NDC 55154-2134-05 None of these listed
Show 3 ingredients

HYDROCHLORIC ACID, SODIUM CHLORIDE, WATER
Chartwell RX, LLC 1 product
0.5 mg/2.5 mL inhalation solution (nebulizer)NDC 62135-0830-84 None of these listed
Show 3 ingredients

HYDROCHLORIC ACID, SODIUM CHLORIDE, WATER
Hikma Pharmaceuticals USA Inc. 2 products
21 mcg nasal sprayNDC 00054-0045-44 Still being read Not read yet
42 mcg nasal sprayNDC 00054-0046-41 None of these listed
Show 7 ingredients

BENZALKONIUM CHLORIDE, EDETATE CALCIUM DISODIUM, HYDROCHLORIC ACID, HYDROXYETHYL CELLULOSE (140 MPA.S AT 5%), SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER
Lupin Pharmaceuticals, Inc. 2 products
21 mcg nasal sprayNDC 70748-0336-01 Still being read Not read yet
42 mcg nasal sprayNDC 70748-0337-01 Still being read Not read yet
Mylan Pharmaceuticals Inc. 1 product
0.5 mg/2.5 mL inhalation solution (nebulizer)NDC 00378-7970-52 None of these listed
Show 3 ingredients

HYDROCHLORIC ACID, SODIUM CHLORIDE, WATER
Nephron Pharmaceuticals Corporation 1 product
0.5 mg/2.5 mL inhalation solution (nebulizer)NDC 00487-9801-01 None of these listed
Show 3 ingredients

HYDROCHLORIC ACID, SODIUM CHLORIDE, WATER
Northstar Rx Llc 2 products
21 mcg nasal sprayNDC 16714-0526-01 None of these listed
Show 6 ingredients

BENZALKONIUM CHLORIDE, EDETATE DISODIUM, HYDROCHLORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER
42 mcg nasal sprayNDC 16714-0527-01 None of these listed
Show 6 ingredients

BENZALKONIUM CHLORIDE, EDETATE DISODIUM, HYDROCHLORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER
NuCare Pharmaceuticals, Inc. 1 product
0.5 mg/2.5 mL inhalation solution (nebulizer)NDC 68071-3769-02 None of these listed
Show 3 ingredients

HYDROCHLORIC ACID, SODIUM CHLORIDE, WATER
Oceanside Pharmaceuticals 1 product
42 mcg nasal sprayNDC 68682-0399-15 None of these listed
Show 6 ingredients

BENZALKONIUM CHLORIDE, EDETATE DISODIUM, HYDROCHLORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER
Redpharm Drug 1 product
0.5 mg/2.5 mL inhalation solution (nebulizer)NDC 67296-2246-01 None of these listed
Show 3 ingredients

HYDROCHLORIC ACID, SODIUM CHLORIDE, WATER
Rising Pharma Holdings, Inc. 1 product
0.5 mg/2.5 mL inhalation solution (nebulizer)NDC 64980-0640-02 None of these listed
Show 3 ingredients

HYDROCHLORIC ACID, SODIUM CHLORIDE, WATER
Ritedose Pharmaceuticals, LLC 1 product
0.5 mg/2.5 mL inhalation solution (nebulizer)NDC 76204-0100-01 None of these listed
Show 3 ingredients

HYDROCHLORIC ACID, SODIUM CHLORIDE, WATER
Sportpharm LLC 1 product
42 mcg nasal sprayNDC 85766-0242-15 None of these listed
Show 6 ingredients

BENZALKONIUM CHLORIDE, EDETATE DISODIUM, HYDROCHLORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER
Sun Pharmaceutical Industries, Inc. 1 product
0.5 mg/2.5 mL inhalation solution (nebulizer)NDC 47335-0706-49 None of these listed
Show 3 ingredients

HYDROCHLORIC ACID, SODIUM CHLORIDE, 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.

Ipratropium without alcohol (ethanol)

Alcohol (ethanol): mostly in liquids; a concern in alcohol recovery, for children, or with disulfiram or metronidazole. 1 of 29 checked products list alcohol (ethanol); 28 do not.

Does not list alcohol (ethanol)

Lists alcohol (ethanol)

At the pharmacy counter

How to use this at the pharmacy counter

  1. 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.
  2. 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.
  3. 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.
  4. 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.
Ask Dr. Staiger which Ipratropium product suits you →

Common questions about Ipratropium inactive ingredients

Is Ipratropium gluten-free?
This page cannot certify any Ipratropium product gluten-free; it reports what each label declares. Of the 29 products checked, none lists a wheat, barley, rye or gluten ingredient, and none lists a starch without a stated source. If you have celiac disease, ask the manufacturer's medical information line for a written gluten statement for the lot you have.
Does Ipratropium contain lactose?
No checked Ipratropium product lists lactose on its label. People with a milk allergy or a strong intolerance often prefer a version that does not list it.
Does Ipratropium contain soy?
No checked Ipratropium product lists a soy ingredient (soybean oil or soy lecithin) on its label. Soy lecithin is the usual form and the amount is small, but people with a soy allergy often prefer a version that does not list it.
Is there a dye-free Ipratropium?
No checked Ipratropium product lists a synthetic dye (an FD&C or D&C colorant) on its label. Colorants often differ by strength within one company's line, so compare the lists above strength by strength.
Does Ipratropium contain gelatin?
No checked Ipratropium product lists gelatin on its label. Gelatin is usually bovine or porcine and the label rarely says which; for kosher, halal or vegetarian needs, ask the manufacturer.
Why do the inactive ingredients differ between manufacturers?
A generic must match the brand's active ingredient, strength, dose form and how it is absorbed; its fillers, binders, coatings and colorants are the manufacturer's own choice. That is why one Ipratropium product can list lactose and a dye while another from a different company lists neither.
Can my pharmacy give me a specific manufacturer's version?
Often, if you ask before the prescription is filled: many pharmacies order from wholesalers that carry several companies' versions and can request a particular one. Some pharmacies buy a generic from one contracted source only, and a few insurance plans cover only certain NDCs, so ask the pharmacist to check. Give them the NDC from this page; the company name alone is often enough.
How current is this list?
The products are the ones in the FDA's current NDC directory as of October 5, 2026, and each inactive-ingredient list is the manufacturer's FDA label as our label sync last read it. Formulations change, so check the label on your own bottle and ask your pharmacist if a refill looks different.

Sources: the products are the finished Ipratropium 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 Ipratropium guide