Inactive ingredients by manufacturer

Atropine inactive ingredients by manufacturer

Wondering whether your Atropine 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 Atropine 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 61 of the 78 current Atropine products on the market today, from 30 companies listing it with the FDA, and lined them up side by side. 16 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 Atropine? 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 Atropine products list lactose, a gluten source, soy, dyes or gelatin?

  1. LactoseNo checked product

    No checked Atropine product lists lactose.

  2. Wheat or gluten sourceNo checked product

    No checked Atropine product lists a wheat or gluten source.

  3. SoyNo checked product

    No checked Atropine product lists soy.

  4. Synthetic dyesNo checked product

    No checked Atropine product lists synthetic dyes.

  5. GelatinNo checked product

    No checked Atropine product lists gelatin.

Also listed by some products: Benzyl alcohol 10 of 61

Find a version without it

Every current Atropine product and what its label lists

Hide products that list:

ProductListsInactive ingredients on the label
A-S Medication Solutions 3 products
10 mg/mL eye dropsNDC 50090-7000-00 None of these listed
Show 8 ingredients

BENZALKONIUM CHLORIDE, EDETATE DISODIUM, HYDROCHLORIC ACID, HYPROMELLOSE 2910 (4000 MPA.S), SODIUM HYDROXIDE, SODIUM PHOSPHATE, DIBASIC, UNSPECIFIED FORM, SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORM, WATER
10 mg/mL eye dropsNDC 50090-7313-00 None of these listed
Show 8 ingredients

BENZALKONIUM CHLORIDE, EDETATE DISODIUM, HYDROCHLORIC ACID, HYPROMELLOSE 2910 (4000 MPA.S), SODIUM HYDROXIDE, SODIUM PHOSPHATE, DIBASIC, SODIUM PHOSPHATE, MONOBASIC, WATER
0.1 mg/mL injectionNDC 50090-5924-00 Still being read Not read yet
Accord Healthcare, Inc., 2 products
0.05 mg/mL injectionNDC 16729-0483-03 None of these listed
Show 4 ingredients

SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER
0.1 mg/mL injectionNDC 16729-0484-03 Still being read Not read yet
Accord Healthcare Inc. 1 product
0.4 mg/mL injectionNDC 16729-0512-43 Still being read Not read yet
Alcon Laboratories, Inc. 2 products
10 mg/mL eye dropsNDC 00065-0303-55 None of these listed
Show 6 ingredients

Benzalkonium Chloride, Boric Acid, Hydrochloric Acid, Hypromelloses, Sodium Hydroxide, Water
10 mg/mL eye dropsNDC 00065-0817-01 None of these listed
Show 6 ingredients

Benzalkonium Chloride, Boric Acid, Hydrochloric Acid, Hypromellose, Unspecified, Sodium Hydroxide, Water
American Regent, Inc. 2 products
0.4 mg/mL injectionNDC 00517-1004-25 None of these listed
Show 4 ingredients

SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER
1 mg/mL injectionNDC 00517-1001-25 None of these listed
Show 4 ingredients

SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER
Amneal Pharmaceuticals LLC 2 products
0.1 mg/mL injectionNDC 70121-1705-07 None of these listed
Show 4 ingredients

SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER
0.1 mg/mL injectionNDC 70121-1706-01 None of these listed
Show 4 ingredients

SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER
Amneal Pharmaceuticals NY LLC 3 products
10 mg/mL eye dropsNDC 60219-1748-02 None of these listed
Show 8 ingredients

BENZALKONIUM CHLORIDE, EDETATE DISODIUM, HYDROCHLORIC ACID, HYPROMELLOSE 2910 (4000 MPA.S), SODIUM HYDROXIDE, SODIUM PHOSPHATE, DIBASIC, SODIUM PHOSPHATE, MONOBASIC, WATER
10 mg/mL eye dropsNDC 60219-1749-03 None of these listed
Show 8 ingredients

BENZALKONIUM CHLORIDE, EDETATE DISODIUM, HYDROCHLORIC ACID, HYPROMELLOSE 2910 (4000 MPA.S), SODIUM HYDROXIDE, SODIUM PHOSPHATE, DIBASIC, SODIUM PHOSPHATE, MONOBASIC, WATER
10 mg/mL eye dropsNDC 60219-1750-08 None of these listed
Show 8 ingredients

BENZALKONIUM CHLORIDE, EDETATE DISODIUM, HYDROCHLORIC ACID, HYPROMELLOSE 2910 (4000 MPA.S), SODIUM HYDROXIDE, SODIUM PHOSPHATE, DIBASIC, SODIUM PHOSPHATE, MONOBASIC, WATER
Apotex Corp. 1 product
10 mg/mL eye dropsNDC 60505-6226-00 None of these listed
Show 8 ingredients

BENZALKONIUM CHLORIDE, EDETATE DISODIUM, HYDROCHLORIC ACID, HYPROMELLOSE 2910 (4000 MPA.S), SODIUM HYDROXIDE, SODIUM PHOSPHATE, DIBASIC, UNSPECIFIED FORM, SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORM, WATER
Bausch & Lomb Incorporated 2 products
10 mg/mL eye dropsNDC 24208-0965-01 None of these listed
Show 5 ingredients

BORIC ACID, HYDROCHLORIC ACID, HYPROMELLOSE, UNSPECIFIED, SODIUM HYDROXIDE, WATER
10 mg/g eye ointmentNDC 24208-0825-55 None of these listed
Show 4 ingredients

LANOLIN OIL, MINERAL OIL, PETROLATUM, WATER
Bausch & Lomb Americas Inc. 1 product
10 mg/mL eye dropsNDC 82260-0001-01 None of these listed
Show 5 ingredients

BORIC ACID, HYDROCHLORIC ACID, HYPROMELLOSE, UNSPECIFIED, SODIUM HYDROXIDE, WATER
Edenbridge Pharmaceuticals LLC. 1 product
10 mg/mL eye dropsNDC 42799-0826-01 None of these listed
Show 8 ingredients

BENZALKONIUM CHLORIDE, EDETATE DISODIUM, HYDROCHLORIC ACID, HYPROMELLOSE 2910 (4000 MPA.S), SODIUM HYDROXIDE, SODIUM PHOSPHATE, DIBASIC, SODIUM PHOSPHATE, MONOBASIC, WATER
Fresenius Kabi USA, LLC 1 product
0.4 mg/mL injectionNDC 63323-0580-20 Still being read Not read yet
Gland Pharma Limited 3 products
10 mg/mL eye dropsNDC 68083-0669-01 Still being read Not read yet
10 mg/mL eye dropsNDC 68083-0670-01 None of these listed
Show 8 ingredients

BENZALKONIUM CHLORIDE, EDETATE DISODIUM, HYDROCHLORIC ACID, HYPROMELLOSE 2910 (4000 MPA.S), SODIUM HYDROXIDE, SODIUM PHOSPHATE, DIBASIC, SODIUM PHOSPHATE, MONOBASIC, WATER
10 mg/mL eye dropsNDC 68083-0671-01 Still being read Not read yet
Henry Schein, Inc 1 product
0.4 mg/mL injectionNDC 00404-9802-01 None of these listed
Show 4 ingredients

SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, Water
Henry Schein, Inc. 3 products
0.05 mg/mL injectionNDC 00404-9823-05 No inactive-ingredient list on the label No list we could read
0.1 mg/mL injectionNDC 00404-9784-05 None of these listed
Show 4 ingredients

SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER
0.4 mg/mL injectionNDC 00404-9804-20 Benzyl alcohol
Show 4 ingredients

BENZYL ALCOHOL, SODIUM CHLORIDE, SULFURIC ACID, WATER
HF Acquisition Co., LLC, DBA Health First 1 product
0.1 mg/mL injectionNDC 51662-1208-01 None of these listed
Show 4 ingredients

SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER
HF Acquisition Co. LLC, DBA Health First 1 product
0.1 mg/mL injectionNDC 51662-1207-01 None of these listed
Show 4 ingredients

SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER
HF Acquisition Co LLC, DBA HealthFirst 6 products
0.1 mg/mL injectionNDC 51662-1527-01 None of these listed
Show 3 ingredients

SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID
0.1 mg/mL injectionNDC 51662-1289-01 None of these listed
Show 4 ingredients

SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER
0.4 mg/mL injectionNDC 51662-1311-01 Benzyl alcohol
Show 4 ingredients

BENZYL ALCOHOL, SODIUM CHLORIDE, SULFURIC ACID, WATER
0.4 mg/mL injectionNDC 51662-1619-01 Benzyl alcohol
Show 3 ingredients

BENZYL ALCOHOL, SODIUM CHLORIDE, SULFURIC ACID
0.4 mg/mL injectionNDC 51662-1627-03 Still being read Not read yet
1 mg/mL injectionNDC 51662-1626-03 None of these listed
Show 4 ingredients

SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER
Hikma Pharmaceuticals USA Inc. 3 products
0.4 mg/mL injectionNDC 00641-6251-10 Benzyl alcohol
Show 3 ingredients

BENZYL ALCOHOL, SODIUM CHLORIDE, SULFURIC ACID
0.4 mg/mL injectionNDC 00641-6274-25 None of these listed
Show 4 ingredients

SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER
1 mg/mL injectionNDC 00641-6275-25 None of these listed
Show 4 ingredients

SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER
Hospira, Inc. 2 products
0.05 mg/mL injectionNDC 00409-9630-05 None of these listed
Show 4 ingredients

SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER
0.1 mg/mL injectionNDC 00409-1630-10 None of these listed
Show 4 ingredients

SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER
International Medication Systems, Limited 1 product
0.1 mg/mL injectionNDC 76329-3340-01 Still being read Not read yet
Lifestar Pharma LLC 3 products
10 mg/mL eye dropsNDC 70756-0651-25 None of these listed
Show 7 ingredients

BENZALKONIUM CHLORIDE, EDETATE DISODIUM, HYDROCHLORIC ACID, HYPROMELLOSE 2910 (4000 MPA.S), SODIUM HYDROXIDE, SODIUM PHOSPHATE, DIBASIC, ANHYDROUS, SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE
10 mg/mL eye dropsNDC 70756-0652-25 None of these listed
Show 7 ingredients

BENZALKONIUM CHLORIDE, EDETATE DISODIUM, HYDROCHLORIC ACID, HYPROMELLOSE 2910 (4000 MPA.S), SODIUM HYDROXIDE, SODIUM PHOSPHATE, DIBASIC, ANHYDROUS, SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE
10 mg/mL eye dropsNDC 70756-0653-35 None of these listed
Show 7 ingredients

BENZALKONIUM CHLORIDE, EDETATE DISODIUM, HYDROCHLORIC ACID, HYPROMELLOSE 2910 (4000 MPA.S), SODIUM HYDROXIDE, SODIUM PHOSPHATE, DIBASIC, ANHYDROUS, SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE
Medefil, Inc. 1 product
0.1 mg/mL injectionNDC 64253-0400-91 None of these listed
Show 1 ingredient

SODIUM CHLORIDE
Medical Purchasing Solutions, LLC 9 products
0.1 mg/mL injectionNDC 71872-7252-01 None of these listed
Show 3 ingredients

SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID
0.1 mg/mL injectionNDC 71872-7298-01 Still being read Not read yet
0.1 mg/mL injectionNDC 71872-7002-01 Still being read Not read yet
0.4 mg/mL injectionNDC 71872-7037-01 Benzyl alcohol
Show 4 ingredients

BENZYL ALCOHOL, SODIUM CHLORIDE, SULFURIC ACID, WATER
0.4 mg/mL injectionNDC 71872-7316-01 Still being read Not read yet
0.4 mg/mL injectionNDC 71872-7312-01 Still being read Not read yet
0.4 mg/mL injectionNDC 71872-7341-01 None of these listed
Show 4 ingredients

SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER
0.4 mg/mL injectionNDC 71872-7355-01 Benzyl alcohol
Show 4 ingredients

BENZYL ALCOHOL, SODIUM CHLORIDE, SULFURIC ACID, WATER
1 mg/mL injectionNDC 71872-7340-01 Still being read Not read yet
Meridian Medical Technologies LLC 5 products
0.5 mg/0.7 mL injectionNDC 11704-0104-01 None of these listed
Show 6 ingredients

citric acid monohydrate, glycerin, Nitrogen, phenol, sodium citrate, unspecified form, water
0.25 mg/0.3 mL injectionNDC 11704-0107-01 None of these listed
Show 5 ingredients

citric acid monohydrate, Nitrogen, sodium chloride, sodium citrate, unspecified form, water
1 mg/0.7 mL injectionNDC 11704-0105-01 None of these listed
Show 6 ingredients

citric acid monohydrate, glycerin, Nitrogen, phenol, sodium citrate, unspecified form, water
2 mg/0.7 mL injectionNDC 11704-0101-01 Still being read Not read yet
2 mg/0.7 mL injectionNDC 11704-0106-01 Still being read Not read yet
NorthStar RxLLC 1 product
10 mg/mL eye dropsNDC 72603-0264-01 None of these listed
Show 7 ingredients

BENZALKONIUM CHLORIDE, EDETATE DISODIUM, HYDROCHLORIC ACID, HYPROMELLOSE 2910 (4000 MPA.S), SODIUM HYDROXIDE, SODIUM PHOSPHATE, DIBASIC, ANHYDROUS, SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE
ProPharma Distribution 5 products
0.1 mg/mL injectionNDC 84549-0340-01 None of these listed
Show 3 ingredients

SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID
0.1 mg/mL injectionNDC 84549-0400-91 None of these listed
Show 1 ingredient

SODIUM CHLORIDE
0.4 mg/mL injectionNDC 84549-0580-20 Benzyl alcohol
Show 4 ingredients

BENZYL ALCOHOL, SODIUM CHLORIDE, SULFURIC ACID, WATER
0.4 mg/mL injectionNDC 84549-0631-25 None of these listed
Show 4 ingredients

SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER
1 mg/mL injectionNDC 84549-0001-25 None of these listed
Show 4 ingredients

SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER
Redpharm Drug 2 products
10 mg/mL eye dropsNDC 67296-2124-05 None of these listed
Show 7 ingredients

BENZALKONIUM CHLORIDE, EDETATE DISODIUM, HYDROCHLORIC ACID, HYPROMELLOSE 2910 (4000 MPA.S), SODIUM HYDROXIDE, SODIUM PHOSPHATE, DIBASIC, ANHYDROUS, SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE
10 mg/mL eye dropsNDC 67296-2200-05 None of these listed
Show 8 ingredients

BENZALKONIUM CHLORIDE, EDETATE DISODIUM, HYDROCHLORIC ACID, HYPROMELLOSE 2910 (4000 MPA.S), SODIUM HYDROXIDE, SODIUM PHOSPHATE, DIBASIC, UNSPECIFIED FORM, SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORM, WATER
Remedyrepack Inc. 3 products
0.1 mg/mL injectionNDC 70518-3120-00 None of these listed
Show 3 ingredients

SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID
0.4 mg/mL injectionNDC 70518-4329-00 Benzyl alcohol
Show 3 ingredients

BENZYL ALCOHOL, SODIUM CHLORIDE, SULFURIC ACID
0.4 mg/mL injectionNDC 70518-4188-00 Benzyl alcohol
Show 4 ingredients

BENZYL ALCOHOL, SODIUM CHLORIDE, SULFURIC ACID, WATER
Somerset Therapeutics, LLC 7 products
10 mg/mL eye dropsNDC 70069-0581-01 None of these listed
Show 6 ingredients

BENZALKONIUM CHLORIDE, EDETATE SODIUM, HYDROCHLORIC ACID, SODIUM HYDROXIDE, SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE, SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE
10 mg/mL eye dropsNDC 70069-0582-01 None of these listed
Show 6 ingredients

BENZALKONIUM CHLORIDE, EDETATE SODIUM, HYDROCHLORIC ACID, SODIUM HYDROXIDE, SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE, SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE
10 mg/mL eye dropsNDC 70069-0583-01 None of these listed
Show 6 ingredients

BENZALKONIUM CHLORIDE, EDETATE SODIUM, HYDROCHLORIC ACID, SODIUM HYDROXIDE, SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE, SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE
10 mg/mL eye dropsNDC 70069-0716-01 None of these listed
Show 6 ingredients

BENZALKONIUM CHLORIDE, BORIC ACID, HYDROCHLORIC ACID, HYPROMELLOSE, UNSPECIFIED, SODIUM HYDROXIDE, WATER
0.4 mg/mL injectionNDC 70069-0481-10 Benzyl alcohol
Show 4 ingredients

BENZYL ALCOHOL, SODIUM CHLORIDE, SULFURIC ACID, WATER
0.4 mg/mL injectionNDC 70069-0631-25 None of these listed
Show 4 ingredients

SODIUM CHLORIDE, SODIUM HYDROXIDE, SULFURIC ACID, WATER
1 mg/mL injectionNDC 70069-0641-25 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.

Atropine without benzyl alcohol

Benzyl alcohol: A preservative, mostly in injections and liquids; not for newborns. 10 of 61 checked products list benzyl alcohol; 51 do not.

Does not list benzyl alcohol

Lists benzyl alcohol

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 Atropine product suits you →

Common questions about Atropine inactive ingredients

Is Atropine gluten-free?
This page cannot certify any Atropine product gluten-free; it reports what each label declares. Of the 61 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 Atropine contain lactose?
No checked Atropine 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 Atropine contain soy?
No checked Atropine 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 Atropine?
No checked Atropine 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 Atropine contain gelatin?
No checked Atropine 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 Atropine 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 September 27, 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 Atropine products in the FDA's current NDC directory (openFDA), as of September 27, 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 Atropine guide