Inactive ingredients by manufacturer

Etomidate inactive ingredients by manufacturer

Wondering whether your Etomidate 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 Etomidate 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 19 of the 24 current Etomidate products on the market today, from 12 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.

Ask about your bottle

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

  1. LactoseNo checked product

    No checked Etomidate product lists lactose.

  2. Wheat or gluten sourceNo checked product

    No checked Etomidate product lists a wheat or gluten source.

  3. SoyNo checked product

    No checked Etomidate product lists soy.

  4. Synthetic dyesNo checked product

    No checked Etomidate product lists synthetic dyes.

  5. GelatinNo checked product

    No checked Etomidate product lists gelatin.

Also listed by some products: Propylene glycol 18 of 19

Find a version without it

Every current Etomidate product and what its label lists

Hide products that list:

ProductListsInactive ingredients on the label
Armas Pharmaceuticals Inc. 2 products
2 mg/mL injectionNDC 72485-0508-10 Propylene glycol
Show 2 ingredients

PROPYLENE GLYCOL, WATER

2 mg/mL injectionNDC 72485-0509-10 Still being read Not read yet
Caplin Steriles Limited 2 products
2 mg/mL injectionNDC 65145-0127-10 Propylene glycol
Show 2 ingredients

PROPYLENE GLYCOL, WATER

2 mg/mL injectionNDC 65145-0128-10 Still being read Not read yet
Civica, Inc. 2 products
2 mg/mL injectionNDC 72572-0161-10 Still being read Not read yet
2 mg/mL injectionNDC 72572-0160-10 Propylene glycol
Show 1 ingredient

PROPYLENE GLYCOL

Eugia US LLC 2 products
20 mg/10 mL injectionNDC 55150-0221-10 Propylene glycol
Show 2 ingredients

PROPYLENE GLYCOL, WATER

40 mg/20 mL injectionNDC 55150-0222-20 Propylene glycol
Show 2 ingredients

PROPYLENE GLYCOL, WATER

Fosun Pharma USA Inc 2 products
2 mg/mL injectionNDC 72266-0147-10 Propylene glycol
Show 2 ingredients

PROPYLENE GLYCOL, WATER

2 mg/mL injectionNDC 72266-0146-10 Propylene glycol
Show 2 ingredients

PROPYLENE GLYCOL, WATER

Fresenius Kabi USA, LLC 2 products
2 mg/mL injectionNDC 65219-0447-20 Propylene glycol
Show 2 ingredients

PROPYLENE GLYCOL, WATER

2 mg/mL injectionNDC 65219-0445-10 Propylene glycol
Show 2 ingredients

PROPYLENE GLYCOL, WATER

Gland Pharma Limited 2 products
2 mg/mL injectionNDC 68083-0235-10 Propylene glycol
Show 2 ingredients

PROPYLENE GLYCOL, WATER

2 mg/mL injectionNDC 68083-0234-10 Propylene glycol
Show 2 ingredients

PROPYLENE GLYCOL, WATER

Henry Schein, Inc. 1 product
2 mg/mL injectionNDC 00404-9811-10 None of these listed
Show 1 ingredient

WATER

HF Acquisition Co LLC, DBA HealthFirst 2 products
2 mg/mL injectionNDC 51662-1485-01 Propylene glycol
Show 1 ingredient

PROPYLENE GLYCOL

40 mg/20 mL injectionNDC 51662-1542-01 Propylene glycol
Show 2 ingredients

PROPYLENE GLYCOL, WATER

Hikma Pharmaceuticals USA Inc. 4 products
2 mg/mL injectionNDC 00143-9310-10 Propylene glycol
Show 1 ingredient

PROPYLENE GLYCOL

2 mg/mL injectionNDC 00143-9311-10 Still being read Not read yet
2 mg/mL injectionNDC 00143-9506-10 Propylene glycol
Show 1 ingredient

PROPYLENE GLYCOL

2 mg/mL injectionNDC 00143-9507-10 Propylene glycol
Show 1 ingredient

PROPYLENE GLYCOL

Hospira, Inc. 1 product
2 mg/mL injectionNDC 00409-6695-01 Propylene glycol
Show 2 ingredients

PROPYLENE GLYCOL, WATER

Mylan Institutional LLC 2 products
2 mg/mL injectionNDC 67457-0902-10 Still being read Not read yet
2 mg/mL injectionNDC 67457-0903-20 Propylene glycol
Show 1 ingredient

PROPYLENE GLYCOL

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.

Etomidate without propylene glycol

Propylene glycol: A solvent in liquids and capsules; a concern in kidney disease, for infants, and at high doses. 18 of 19 checked products list propylene glycol; 1 does not.

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 Etomidate product suits you →

Common questions about Etomidate inactive ingredients

Is Etomidate gluten-free?
This page cannot certify any Etomidate product gluten-free; it reports what each label declares. Of the 19 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 Etomidate contain lactose?
No checked Etomidate 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 Etomidate contain soy?
No checked Etomidate 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 Etomidate?
No checked Etomidate 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 Etomidate contain gelatin?
No checked Etomidate 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 October 6, 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 Etomidate products in the FDA's current NDC directory (openFDA), as of October 6, 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 Etomidate guide