Inactive ingredients by manufacturer

Heparin inactive ingredients by manufacturer

Wondering whether your Heparin 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 Heparin 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 107 of the 119 current Heparin products on the market today, from 26 companies listing it with the FDA, and lined them up side by side. 10 are still being read and will appear on a later visit. 2 labels have no inactive-ingredient list we could read, so those products cannot be compared.

Ask about your bottle

Is there something in your Heparin? 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 Heparin products list lactose, a gluten source, soy, dyes or gelatin?

  1. LactoseNo checked product

    No checked Heparin product lists lactose.

  2. Wheat or gluten sourceNo checked product

    No checked Heparin product lists a wheat or gluten source.

  3. SoyNo checked product

    No checked Heparin product lists soy.

  4. Synthetic dyesNo checked product

    No checked Heparin product lists synthetic dyes.

  5. GelatinNo checked product

    No checked Heparin product lists gelatin.

Also listed by some products: Sulfites 3 of 107 Benzyl alcohol 39 of 107 Sugar 3 of 107

Find a version without it

Every current Heparin product and what its label lists

Hide products that list:

ProductListsInactive ingredients on the label
B. Braun Medical Inc. 3 products
200 [USP'U]/100 mL injectionNDC 00264-9872-00 None of these listed
Show 4 ingredients

ANHYDROUS CITRIC ACID, SODIUM CHLORIDE, SODIUM PHOSPHATE, DIBASIC, WATER
5000 [USP'U]/100 mL injectionNDC 00264-3301-10 None of these listed
Show 4 ingredients

ANHYDROUS CITRIC ACID, SODIUM CHLORIDE, SODIUM PHOSPHATE, DIBASIC, WATER
10000 [USP'U]/100 mL injectionNDC 00264-3462-20 None of these listed
Show 4 ingredients

ANHYDROUS CITRIC ACID, SODIUM CHLORIDE, SODIUM PHOSPHATE, DIBASIC, WATER
Baxter Healthcare Corporation 4 products
200 [USP'U]/100 mL injectionNDC 00338-0424-18 None of these listed
Show 4 ingredients

CITRIC ACID MONOHYDRATE, SODIUM CHLORIDE, SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE, WATER
200 [USP'U]/100 mL injectionNDC 00338-0428-12 None of these listed
Show 4 ingredients

CITRIC ACID MONOHYDRATE, SODIUM CHLORIDE, SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE, WATER
200 [USP'U]/100 mL injectionNDC 00338-0431-03 None of these listed
Show 4 ingredients

CITRIC ACID MONOHYDRATE, SODIUM CHLORIDE, SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE, WATER
200 [USP'U]/100 mL injectionNDC 00338-0433-04 None of these listed
Show 4 ingredients

CITRIC ACID MONOHYDRATE, SODIUM CHLORIDE, SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE, WATER
BE Pharmaceuticals Inc. 2 products
2000 [USP'U]/2 mL injectionNDC 71839-0117-25 None of these listed
Show 4 ingredients

HYDROCHLORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER
5000 [USP'U]/0.5 mL injectionNDC 71839-0118-25 None of these listed
Show 3 ingredients

HYDROCHLORIC ACID, SODIUM HYDROXIDE, WATER
Cardinal Health 107, LLC 7 products
1000 [USP'U]/mL injectionNDC 55154-9583-05 Still being read Not read yet
5000 [USP'U]/0.5 mL injectionNDC 55154-9589-05 None of these listed
Show 1 ingredient

WATER
5000 [USP'U]/mL injectionNDC 55154-5130-05 Benzyl alcohol
Show 2 ingredients

BENZYL ALCOHOL, SODIUM CHLORIDE
5000 [USP'U]/mL injectionNDC 55154-9585-05 None of these listed
Show 4 ingredients

METHYLPARABEN, PROPYLPARABEN, SODIUM CHLORIDE, WATER
5000 [USP'U]/mL injectionNDC 55154-2827-05 Benzyl alcohol
Show 4 ingredients

BENZYL ALCOHOL, NITROGEN, SODIUM CHLORIDE, WATER
5000 [USP'U]/mL injectionNDC 55154-6985-05 Benzyl alcohol
Show 3 ingredients

BENZYL ALCOHOL, SODIUM CHLORIDE, WATER
10000 [USP'U]/mL injectionNDC 55154-2380-05 None of these listed
Show 1 ingredient

WATER
Civica, Inc. 2 products
1000 [USP'U]/mL injectionNDC 72572-0250-25 Benzyl alcohol
Show 2 ingredients

BENZYL ALCOHOL, SODIUM CHLORIDE
5000 [USP'U]/mL injectionNDC 72572-0255-25 Benzyl alcohol
Show 2 ingredients

BENZYL ALCOHOL, SODIUM CHLORIDE
Fresenius Kabi USA, LLC 16 products
200 [USP'U]/100 mL injectionNDC 63323-0519-10 None of these listed
Show 3 ingredients

Anhydrous Citric Acid, Sodium Chloride, Sodium Phosphate, Dibasic, Heptahydrate
1000 [USP'U]/mL injectionNDC 63323-0276-02 None of these listed
Show 3 ingredients

HYDROCHLORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE
1000 [USP'U]/mL injectionNDC 63323-0540-01 None of these listed
Show 5 ingredients

HYDROCHLORIC ACID, METHYLPARABEN, PROPYLPARABEN, SODIUM CHLORIDE, SODIUM HYDROXIDE
1000 [USP'U]/mL injectionNDC 65219-0066-10 None of these listed
Show 6 ingredients

HYDROCHLORIC ACID, METHYLPARABEN, PROPYLPARABEN, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER
5000 [USP'U]/0.5 mL injectionNDC 63323-0118-05 None of these listed
Show 4 ingredients

Hydrochloric Acid, Sodium Chloride, Sodium Hydroxide, Water
5000 [USP'U]/0.5 mL injectionNDC 63323-0543-02 None of these listed
Show 2 ingredients

HYDROCHLORIC ACID, SODIUM HYDROXIDE
5000 [USP'U]/100 mL injectionNDC 63323-0518-77 None of these listed
Show 3 ingredients

EDETATE DISODIUM, SODIUM CHLORIDE, WATER
5000 [USP'U]/100 mL injectionNDC 63323-0522-77 Sulfites Sugar (sucrose, dextrose)
Show 4 ingredients

ANHYDROUS CITRIC ACID, DEXTROSE MONOHYDRATE, SODIUM METABISULFITE, TRISODIUM CITRATE DIHYDRATE
5000 [USP'U]/mL injectionNDC 76045-0108-10 None of these listed
Show 4 ingredients

HYDROCHLORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER
5000 [USP'U]/mL injectionNDC 63323-0047-10 Benzyl alcohol
Show 4 ingredients

BENZYL ALCOHOL, HYDROCHLORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE
5000 [USP'U]/mL injectionNDC 63323-0262-01 None of these listed
Show 5 ingredients

HYDROCHLORIC ACID, METHYLPARABEN, PROPYLPARABEN, SODIUM CHLORIDE, SODIUM HYDROXIDE
10000 [USP'U]/100 mL injectionNDC 63323-0517-74 None of these listed
Show 5 ingredients

EDETATE DISODIUM, HYDROCHLORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER
10000 [USP'U]/100 mL injectionNDC 63323-0523-74 Sulfites Sugar (sucrose, dextrose)
Show 4 ingredients

ANHYDROUS CITRIC ACID, DEXTROSE MONOHYDRATE, SODIUM METABISULFITE, TRISODIUM CITRATE DIHYDRATE
10000 [USP'U]/mL injectionNDC 63323-0459-09 Benzyl alcohol
Show 4 ingredients

BENZYL ALCOHOL, HYDROCHLORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE
10000 [USP'U]/mL injectionNDC 63323-0542-01 None of these listed
Show 4 ingredients

HYDROCHLORIC ACID, METHYLPARABEN, PROPYLPARABEN, SODIUM HYDROXIDE
20000 [USP'U]/mL injectionNDC 63323-0915-01 None of these listed
Show 4 ingredients

HYDROCHLORIC ACID, METHYLPARABEN, PROPYLPARABEN, SODIUM HYDROXIDE
Gland Pharma Limited 3 products
1000 [USP'U]/mL injectionNDC 68083-0427-25 Benzyl alcohol
Show 2 ingredients

BENZYL ALCOHOL, SODIUM CHLORIDE
1000 [USP'U]/mL injectionNDC 68083-0428-25 Benzyl alcohol
Show 2 ingredients

BENZYL ALCOHOL, SODIUM CHLORIDE
5000 [USP'U]/mL injectionNDC 68083-0136-25 Benzyl alcohol
Show 2 ingredients

BENZYL ALCOHOL, SODIUM CHLORIDE
Henry Schein, Inc. 2 products
1000 [USP'U]/mL injectionNDC 00404-9979-01 None of these listed
Show 5 ingredients

HYDROCHLORIC ACID, METHYLPARABEN, PROPYLPARABEN, SODIUM CHLORIDE, SODIUM HYDROXIDE
5000 [USP'U]/mL injectionNDC 00404-9872-01 No inactive-ingredient list on the label No list we could read
Hepalink USA Inc. 6 products
1000 [USP'U]/mL injectionNDC 81952-0112-06 None of these listed
Show 6 ingredients

HYDROCHLORIC ACID, METHYLPARABEN, PROPYLPARABEN, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER
1000 [USP'U]/mL injectionNDC 81952-0115-07 None of these listed
Show 4 ingredients

HYDROCHLORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER
5000 [USP'U]/mL injectionNDC 81952-0114-09 Benzyl alcohol
Show 5 ingredients

BENZYL ALCOHOL, HYDROCHLORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER
5000 [USP'U]/mL injectionNDC 81952-0111-06 None of these listed
Show 6 ingredients

HYDROCHLORIC ACID, METHYLPARABEN, PROPYLPARABEN, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER
10000 [USP'U]/mL injectionNDC 81952-0113-06 None of these listed
Show 5 ingredients

HYDROCHLORIC ACID, METHYLPARABEN, PROPYLPARABEN, SODIUM HYDROXIDE, WATER
20000 [USP'U]/mL injectionNDC 81952-0116-06 None of these listed
Show 5 ingredients

HYDROCHLORIC ACID, METHYLPARABEN, PROPYLPARABEN, SODIUM HYDROXIDE, WATER
HF Acquisition Co LLC, DBA HealthFirst 6 products
5000 [USP'U]/mL injectionNDC 51662-1460-01 Benzyl alcohol
Show 4 ingredients

BENZYL ALCOHOL, HYDROCHLORIC ACID, SODIUM HYDROXIDE, WATER
10000 [USP'U]/100 mL injectionNDC 51662-1578-01 None of these listed
Show 5 ingredients

EDETATE DISODIUM, HYDROCHLORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER
10000 [USP'U]/100 mL injectionNDC 51662-1687-03 None of these listed
Show 5 ingredients

EDETATE DISODIUM ANHYDROUS, HYDROCHLORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER
10000 [USP'U]/mL injectionNDC 51662-1409-01 None of these listed
Show 4 ingredients

HYDROCHLORIC ACID, METHYLPARABEN, PROPYLPARABEN, SODIUM HYDROXIDE
10000 [USP'U]/mL injectionNDC 51662-1434-01 None of these listed
Show 5 ingredients

HYDROCHLORIC ACID, METHYLPARABEN, PROPYLPARABEN, SODIUM HYDROXIDE, WATER
10000 [USP'U]/mL injectionNDC 51662-1486-01 Benzyl alcohol
Show 5 ingredients

BENZYL ALCOHOL, HYDROCHLORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER
Hikma Pharmaceuticals USA Inc. 5 products
1000 [USP'U]/mL injectionNDC 00641-0391-12 Benzyl alcohol
Show 2 ingredients

BENZYL ALCOHOL, SODIUM CHLORIDE
5000 [USP'U]/0.5 mL injectionNDC 00641-6204-10 No inactive-ingredient list on the label No list we could read
5000 [USP'U]/mL injectionNDC 00641-0400-12 Benzyl alcohol
Show 2 ingredients

BENZYL ALCOHOL, SODIUM CHLORIDE
5000 [USP'U]/mL injectionNDC 00641-6199-10 None of these listed
Show 1 ingredient

SODIUM CHLORIDE
10000 [USP'U]/mL injectionNDC 00641-0410-12 Still being read Not read yet
Hospira, Inc. 10 products
200 [USP'U]/100 mL injectionNDC 00409-1005-20 None of these listed
Show 4 ingredients

CITRIC ACID MONOHYDRATE, SODIUM CHLORIDE, SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE, WATER
200 [USP'U]/100 mL injectionNDC 00409-2222-12 None of these listed
Show 4 ingredients

CITRIC ACID MONOHYDRATE, SODIUM CHLORIDE, SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE, WATER
1000 [USP'U]/mL injectionNDC 00409-2720-01 Benzyl alcohol
Show 5 ingredients

BENZYL ALCOHOL, HYDROCHLORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER
5000 [USP'U]/100 mL injectionNDC 00409-0012-30 None of these listed
Show 5 ingredients

EDETATE DISODIUM ANHYDROUS, HYDROCHLORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER
5000 [USP'U]/100 mL injectionNDC 00409-3150-20 None of these listed
Show 5 ingredients

EDETATE DISODIUM ANHYDROUS, HYDROCHLORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER
5000 [USP'U]/mL injectionNDC 00409-2723-01 Benzyl alcohol
Show 5 ingredients

BENZYL ALCOHOL, HYDROCHLORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER
10000 [USP'U]/100 mL injectionNDC 00409-4520-30 Sulfites Sugar (sucrose, dextrose)
Show 4 ingredients

ANHYDROUS CITRIC ACID, DEXTROSE MONOHYDRATE, SODIUM METABISULFITE, TRISODIUM CITRATE DIHYDRATE
10000 [USP'U]/100 mL injectionNDC 00409-7650-30 None of these listed
Show 5 ingredients

EDETATE DISODIUM ANHYDROUS, HYDROCHLORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER
10000 [USP'U]/mL injectionNDC 00409-1316-32 None of these listed
Show 3 ingredients

HYDROCHLORIC ACID, SODIUM HYDROXIDE, WATER
10000 [USP'U]/mL injectionNDC 00409-2721-01 Benzyl alcohol
Show 5 ingredients

BENZYL ALCOHOL, HYDROCHLORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER
McKesson Corporation dba SKY Packaging 9 products
1000 [USP'U]/mL injectionNDC 63739-0900-26 Still being read Not read yet
1000 [USP'U]/mL injectionNDC 63739-0920-25 Still being read Not read yet
1000 [USP'U]/mL injectionNDC 63739-0931-28 None of these listed
Show 6 ingredients

HYDROCHLORIC ACID, METHYLPARABEN, PROPYLPARABEN, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER
1000 [USP'U]/mL injectionNDC 63739-0942-29 None of these listed
Show 6 ingredients

HYDROCHLORIC ACID, METHYLPARABEN, PROPYLPARABEN, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER
5000 [USP'U]/mL injectionNDC 63739-0901-28 Benzyl alcohol
Show 5 ingredients

BENZYL ALCOHOL, HYDROCHLORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER
5000 [USP'U]/mL injectionNDC 63739-0953-25 None of these listed
Show 6 ingredients

HYDROCHLORIC ACID, METHYLPARABEN, PROPYLPARABEN, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER
10000 [USP'U]/mL injectionNDC 63739-0964-25 None of these listed
Show 5 ingredients

HYDROCHLORIC ACID, METHYLPARABEN, PROPYLPARABEN, SODIUM HYDROXIDE, WATER
10000 [USP'U]/mL injectionNDC 63739-0975-27 None of these listed
Show 5 ingredients

HYDROCHLORIC ACID, METHYLPARABEN, PROPYLPARABEN, SODIUM HYDROXIDE, WATER
20000 [USP'U]/mL injectionNDC 63739-0986-25 None of these listed
Show 5 ingredients

HYDROCHLORIC ACID, METHYLPARABEN, PROPYLPARABEN, SODIUM HYDROXIDE, WATER
Medical Purchasing Solutions, LLC 3 products
1000 [USP'U]/mL injectionNDC 71872-7352-01 Benzyl alcohol
Show 5 ingredients

BENZYL ALCOHOL, HYDROCHLORIC ACID, NITROGEN, SODIUM HYDROXIDE, WATER
1000 [USP'U]/mL injectionNDC 71872-7364-01 Still being read Not read yet
1000 [USP'U]/mL injectionNDC 71872-7365-01 Still being read Not read yet
Medical Purchasing Solutions, LLC. 1 product
1000 [USP'U]/mL injectionNDC 71872-7351-01 Still being read Not read yet
Meitheal Pharmaceuticals Inc. 10 products
1000 [USP'U]/mL injectionNDC 71288-0449-02 Benzyl alcohol
Show 5 ingredients

benzyl alcohol, hydrochloric acid, nitrogen, sodium hydroxide, water
1000 [USP'U]/mL injectionNDC 71288-0402-02 Benzyl alcohol
Show 5 ingredients

benzyl alcohol, hydrochloric acid, nitrogen, sodium hydroxide, water
2000 [USP'U]/2 mL injectionNDC 71288-0400-03 None of these listed
Show 4 ingredients

hydrochloric acid, sodium chloride, sodium hydroxide, water
5000 [USP'U]/0.5 mL injectionNDC 71288-0405-81 None of these listed
Show 3 ingredients

hydrochloric acid, sodium hydroxide, water
5000 [USP'U]/mL injectionNDC 71288-0450-02 Benzyl alcohol
Show 5 ingredients

benzyl alcohol, hydrochloric acid, nitrogen, sodium hydroxide, water
5000 [USP'U]/mL injectionNDC 71288-0403-02 Benzyl alcohol
Show 5 ingredients

benzyl alcohol, hydrochloric acid, nitrogen, sodium hydroxide, water
5000 [USP'U]/mL injectionNDC 71288-0406-82 Benzyl alcohol
Show 5 ingredients

benzyl alcohol, hydrochloric acid, sodium chloride, sodium hydroxide, water
10000 [USP'U]/mL injectionNDC 71288-0451-02 Benzyl alcohol
Show 5 ingredients

benzyl alcohol, hydrochloric acid, nitrogen, sodium hydroxide, water
10000 [USP'U]/mL injectionNDC 71288-0404-02 Benzyl alcohol
Show 5 ingredients

benzyl alcohol, hydrochloric acid, nitrogen, sodium hydroxide, water
20000 [USP'U]/mL injectionNDC 71288-0401-02 Benzyl alcohol
Show 5 ingredients

benzyl alcohol, hydrochloric acid, nitrogen, sodium hydroxide, water
Mylan Institutional LLC 1 product
1000 [USP'U]/mL injectionNDC 67457-0384-99 Still being read Not read yet
Northstar Rx LLC 3 products
1000 [USP'U]/mL injectionNDC 72603-0250-25 None of these listed
Show 6 ingredients

HYDROCHLORIC ACID, METHYLPARABEN, PROPYLPARABEN, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER
5000 [USP'U]/mL injectionNDC 72603-0456-25 None of these listed
Show 6 ingredients

HYDROCHLORIC ACID, METHYLPARABEN, PROPYLPARABEN, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER
10000 [USP'U]/mL injectionNDC 72603-0579-25 None of these listed
Show 5 ingredients

HYDROCHLORIC ACID, METHYLPARABEN, PROPYLPARABEN, SODIUM HYDROXIDE, WATER
NorthStar RxLLC 8 products
1000 [USP'U]/mL injectionNDC 72603-0267-25 Benzyl alcohol
Show 5 ingredients

benzyl alcohol, hydrochloric acid, nitrogen, sodium hydroxide, water
1000 [USP'U]/mL injectionNDC 72603-0234-25 Still being read Not read yet
1000 [USP'U]/mL injectionNDC 72603-0179-25 Benzyl alcohol
Show 5 ingredients

benzyl alcohol, hydrochloric acid, nitrogen, sodium hydroxide, water
2000 [USP'U]/2 mL injectionNDC 72603-0336-25 None of these listed
Show 4 ingredients

hydrochloric acid, sodium chloride, sodium hydroxide, water
5000 [USP'U]/mL injectionNDC 72603-0412-25 Benzyl alcohol
Show 5 ingredients

benzyl alcohol, hydrochloric acid, nitrogen, sodium hydroxide, water
5000 [USP'U]/mL injectionNDC 72603-0214-25 Benzyl alcohol
Show 5 ingredients

benzyl alcohol, hydrochloric acid, nitrogen, sodium hydroxide, water
10000 [USP'U]/mL injectionNDC 72603-0501-25 Benzyl alcohol
Show 5 ingredients

benzyl alcohol, hydrochloric acid, nitrogen, sodium hydroxide, water
20000 [USP'U]/mL injectionNDC 72603-0224-25 Still being read Not read yet
Pfizer Laboratories Div Pfizer Inc 1 product
1000 [USP'U]/mL injectionNDC 00069-0043-01 None of these listed
Show 4 ingredients

HYDROCHLORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER
Phlow Corporation 1 product
1000 [USP'U]/mL injectionNDC 81565-0203-02 None of these listed
Show 6 ingredients

HYDROCHLORIC ACID, METHYLPARABEN, PROPYLPARABEN, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER
Plano Pharmaceuticals Inc. 1 product
5000 [USP'U]/mL injectionNDC 87188-0102-90 None of these listed
Show 6 ingredients

HYDROCHLORIC ACID, METHYLPARABEN, PROPYLPARABEN, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER
Remedyrepack Inc. 1 product
5000 [USP'U]/mL injectionNDC 70518-4547-00 Benzyl alcohol
Show 2 ingredients

BENZYL ALCOHOL, SODIUM CHLORIDE
Sagent Pharmaceuticals 2 products
1000 [USP'U]/mL injectionNDC 25021-0401-02 None of these listed
Show 4 ingredients

hydrochloric acid, sodium chloride, sodium hydroxide, water
20000 [USP'U]/mL injectionNDC 25021-0404-01 Benzyl alcohol
Show 5 ingredients

benzyl alcohol, hydrochloric acid, nitrogen, sodium hydroxide, water
Sagent Pharmaceticals 3 products
1000 [USP'U]/mL injectionNDC 25021-0400-01 Benzyl alcohol
Show 6 ingredients

Benzyl Alcohol, Hydrochloric Acid, Nitrogen, Sodium Chloride, Sodium Hydroxide, Water
5000 [USP'U]/mL injectionNDC 25021-0402-01 Benzyl alcohol
Show 6 ingredients

Benzyl Alcohol, Hydrochloric Acid, Nitrogen, Sodium Chloride, Sodium Hydroxide, Water
10000 [USP'U]/mL injectionNDC 25021-0403-01 Benzyl alcohol
Show 6 ingredients

Benzyl Alcohol, Hydrochloric Acid, Nitrogen, Sodium Chloride, Sodium Hydroxide, Water
Sandoz Inc. 9 products
1000 [USP'U]/mL injectionNDC 00781-3538-25 None of these listed
Show 6 ingredients

HYDROCHLORIC ACID, METHYLPARABEN, PROPYLPARABEN, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER
1000 [USP'U]/mL injectionNDC 00781-3540-25 None of these listed
Show 6 ingredients

HYDROCHLORIC ACID, METHYLPARABEN, PROPYLPARABEN, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER
1000 [USP'U]/mL injectionNDC 00781-3543-25 None of these listed
Show 6 ingredients

HYDROCHLORIC ACID, METHYLPARABEN, PROPYLPARABEN, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER
1000 [USP'U]/mL injectionNDC 00781-3555-25 None of these listed
Show 4 ingredients

HYDROCHLORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER
5000 [USP'U]/mL injectionNDC 00781-3545-25 None of these listed
Show 6 ingredients

HYDROCHLORIC ACID, METHYLPARABEN, PROPYLPARABEN, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER
5000 [USP'U]/mL injectionNDC 00781-3550-25 Benzyl alcohol
Show 5 ingredients

BENZYL ALCOHOL, HYDROCHLORIC ACID, SODIUM CHLORIDE, SODIUM HYDROXIDE, WATER
10000 [USP'U]/mL injectionNDC 00781-3439-25 None of these listed
Show 5 ingredients

HYDROCHLORIC ACID, METHYLPARABEN, PROPYLPARABEN, SODIUM HYDROXIDE, WATER
10000 [USP'U]/mL injectionNDC 00781-3533-25 None of these listed
Show 5 ingredients

HYDROCHLORIC ACID, METHYLPARABEN, PROPYLPARABEN, SODIUM HYDROXIDE, WATER
20000 [USP'U]/mL injectionNDC 00781-3541-25 None of these listed
Show 5 ingredients

HYDROCHLORIC ACID, METHYLPARABEN, PROPYLPARABEN, SODIUM HYDROXIDE, 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.

Heparin without sulfites

Sulfites: metabisulfite or bisulfite preservatives; a concern with sulfite sensitivity or asthma. 3 of 107 checked products list sulfites; 104 do not.

Does not list sulfites

Lists sulfites

Heparin without benzyl alcohol

Benzyl alcohol: A preservative, mostly in injections and liquids; not for newborns. 39 of 107 checked products list benzyl alcohol; 68 do not.

Does not list benzyl alcohol

Lists benzyl alcohol

Heparin without sugar (sucrose or dextrose)

Sugar (sucrose, dextrose): A consideration in diabetes, mostly in liquids and chewables. 3 of 107 checked products list sugar (sucrose or dextrose); 104 do not.

Does not list sugar (sucrose or dextrose)

Lists sugar (sucrose or dextrose)

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 Heparin product suits you →

Common questions about Heparin inactive ingredients

Is Heparin gluten-free?
This page cannot certify any Heparin product gluten-free; it reports what each label declares. Of the 107 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 Heparin contain lactose?
No checked Heparin 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 Heparin contain soy?
No checked Heparin 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 Heparin?
No checked Heparin 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 Heparin contain gelatin?
No checked Heparin 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 and dose form. For injectable, ophthalmic and otic products the FDA generally requires the inactive ingredients to match the reference product as well, so the lists on this page differ less than they do for tablets and capsules; the differences that remain come from the exact product and container each company files.
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 August 28, 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 Heparin products in the FDA's current NDC directory (openFDA), as of August 28, 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 Heparin guide