Inactive ingredients by manufacturer

Propofol inactive ingredients by manufacturer

Every Propofol product declares its inactive ingredients (excipients) on its FDA label, and the list changes from one company to the next. Find the version that does not list an ingredient you avoid, then take its NDC to your pharmacist.

14 of 14 current Propofol products from 14 companies listing it with the FDA have been read from their FDA labels and compared side by side. The FDA directory lists 35 current products in all; this page compares the 14 in our label sample.

The short answer

Which Propofol products list lactose, a gluten source, dyes or gelatin?

  1. LactoseNo checked product

    No checked Propofol product lists lactose.

  2. Wheat or gluten sourceNo checked product

    No checked Propofol product lists a wheat or gluten source.

  3. Synthetic dyesNo checked product

    No checked Propofol product lists synthetic dyes.

  4. GelatinNo checked product

    No checked Propofol product lists gelatin.

Also listed by some products: Soy 14 of 14 Sulfites 1 of 14 Benzyl alcohol 4 of 14

Find a version without it

Current Propofol products in our label sample and what each label lists

Hide products that list:

ProductListsInactive ingredients on the label
Amneal Pharmaceuticals Private Limited 1 product
10 mg/mL injectionNDC 80830-1188-07 Soy
Show 6 ingredients

EDETATE DISODIUM ANHYDROUS, EGG PHOSPHOLIPIDS, GLYCERIN, SODIUM HYDROXIDE, SOYBEAN OIL, WATER

Anthea Pharma Private Limited 1 product
10 mg/mL injectionNDC 83854-0018-10 Soy
Show 5 ingredients

EDETATE DISODIUM ANHYDROUS, EGG PHOSPHOLIPIDS, GLYCERIN, SODIUM HYDROXIDE, SOYBEAN OIL

Avenacy, LLC 1 product
10 mg/mL injectionNDC 83634-0603-20 Soy
Show 6 ingredients

EDETATE DISODIUM, EGG PHOSPHOLIPIDS, GLYCERIN, SODIUM HYDROXIDE, SOYBEAN OIL, WATER

Civica, Inc 1 product
10 mg/mL injectionNDC 72572-0601-20 Soy
Show 6 ingredients

EDETATE DISODIUM, EGG PHOSPHOLIPIDS, GLYCERIN, SODIUM HYDROXIDE, SOYBEAN OIL, WATER

Dr. Reddy's Laboratories, Inc. 1 product
10 mg/mL injectionNDC 43598-0549-10 Soy Benzyl alcohol
Show 5 ingredients

BENZYL ALCOHOL, EGG PHOSPHOLIPIDS, GLYCERIN, SODIUM HYDROXIDE, SOYBEAN OIL

Fresenius Kabi USA, LLC 1 product
10 mg/mL injectionNDC 65219-0800-10 Soy
Show 5 ingredients

EDETATE DISODIUM ANHYDROUS, EGG PHOSPHOLIPIDS, GLYCERIN, SODIUM HYDROXIDE, SOYBEAN OIL

Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. 1 product
10 mg/mL injectionNDC 23155-0345-41 Soy
Show 6 ingredients

EDETATE DISODIUM, EGG PHOSPHOLIPIDS, GLYCERIN, SODIUM HYDROXIDE, SOYBEAN OIL, WATER

HF Acquisition Co LLC, DBA HealthFirst 1 product
10 mg/mL injectionNDC 51662-1471-01 Soy Benzyl alcohol
Show 6 ingredients

BENZYL ALCOHOL, EGG PHOSPHOLIPIDS, GLYCERIN, SODIUM BENZOATE, SODIUM HYDROXIDE, SOYBEAN OIL

Hikma Pharmaceuticals USA Inc. 1 product
10 mg/mL injectionNDC 00641-6196-10 Soy Benzyl alcohol
Show 4 ingredients

BENZYL ALCOHOL, EGG PHOSPHOLIPIDS, GLYCERIN, SOYBEAN OIL

Hospira, Inc. 1 product
10 mg/mL injectionNDC 00409-0501-98 Soy Benzyl alcohol
Show 6 ingredients

BENZYL ALCOHOL, EGG PHOSPHOLIPIDS, GLYCERIN, SODIUM BENZOATE, SODIUM HYDROXIDE, SOYBEAN OIL

Meitheal Pharmaceuticals Inc. 1 product
10 mg/mL injectionNDC 71288-0731-53 Soy
Show 6 ingredients

EDETATE DISODIUM, EGG PHOSPHOLIPIDS, GLYCERIN, SODIUM HYDROXIDE, SOYBEAN OIL, WATER

NorthStar Rx LLC 1 product
10 mg/mL injectionNDC 16714-0690-10 Soy
Show 6 ingredients

EDETATE DISODIUM, EGG PHOSPHOLIPIDS, GLYCERIN, SODIUM HYDROXIDE, SOYBEAN OIL, WATER

Pfizer Laboratories Div Pfizer Inc 1 product
10 mg/mL injectionNDC 00069-0248-10 Soy
Show 6 ingredients

EDETATE DISODIUM, EGG PHOSPHOLIPIDS, GLYCERIN, SODIUM HYDROXIDE, SOYBEAN OIL, WATER

Sagent Pharmaceuticals 1 product
10 mg/mL injectionNDC 25021-0608-20 Soy Sulfites
Show 5 ingredients

egg phospholipids, glycerin, sodium hydroxide, sodium metabisulfite, soybean oil

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.

Propofol and soy

Soy: soybean oil or soy lecithin; a concern with soy allergy. Every checked Propofol product (14) lists soy.

Lists soy

Propofol without sulfites

Sulfites: metabisulfite or bisulfite preservatives; a concern with sulfite sensitivity or asthma. 1 of 14 checked products list sulfites; 13 do not.

Does not list sulfites

Lists sulfites

Propofol without benzyl alcohol

Benzyl alcohol: A preservative, mostly in injections and liquids; not for newborns. 4 of 14 checked products list benzyl alcohol; 10 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 Propofol product suits you →

Common questions about Propofol inactive ingredients

Is Propofol gluten-free?
This page cannot certify any Propofol product gluten-free; it reports what each label declares. Of the 14 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 Propofol contain lactose?
No checked Propofol product lists lactose on its label. People with a milk allergy or a strong intolerance often prefer a version that does not list it.
Is there a dye-free Propofol?
No checked Propofol 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 Propofol contain gelatin?
No checked Propofol 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 September 24, 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 Propofol products in the FDA's current NDC directory (openFDA), as of September 24, 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 Propofol guide