Atovaquone inactive ingredients by manufacturer
Wondering whether your Atovaquone 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 Atovaquone 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 14 of the 24 current Atovaquone products on the market today, from 21 companies listing it with the FDA, and lined them up side by side. The FDA directory lists 25 current products in all; this page covers the 24 we hold labels for. 9 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 Atovaquone? 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 Atovaquone products list lactose, a gluten source, soy, dyes or gelatin?
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LactoseNo checked product
No checked Atovaquone product lists lactose.
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Wheat or gluten sourceNo checked product
No checked Atovaquone product lists a wheat or gluten source.
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SoyNo checked product
No checked Atovaquone product lists soy.
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Synthetic dyesNo checked product
No checked Atovaquone product lists synthetic dyes.
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GelatinNo checked product
No checked Atovaquone product lists gelatin.
Also listed by some products: Benzyl alcohol 14 of 14 PEG or polysorbate 14 of 14
Find a version without it
Current Atovaquone products in our label sample and what each label lists
| Product | Lists | Inactive ingredients on the label |
|---|---|---|
| A2A Integrated Pharmaceuticals, LLC 1 product | ||
| 750 mg/5 mL oral suspensionNDC 73141-0104-42 | Benzyl alcohol Polyethylene glycol or polysorbate |
Show 7 ingredientsBENZYL ALCOHOL, HYDROCHLORIC ACID, POLOXAMER 188, SACCHARIN SODIUM, SODIUM HYDROXIDE, WATER, XANTHAN GUM |
| Abon Pharmaceuticals, LLC 1 product | ||
| 750 mg/5 mL oral suspensionNDC 42239-0001-08 | Benzyl alcohol Polyethylene glycol or polysorbate |
Show 5 ingredientsBENZYL ALCOHOL, POLOXAMER 188, SACCHARIN SODIUM, WATER, XANTHAN GUM |
| American Health Packaging 1 product | ||
| 750 mg/5 mL oral suspensionNDC 60687-0534-36 | Benzyl alcohol Polyethylene glycol or polysorbate |
Show 6 ingredientsBENZYL ALCOHOL, HYPROMELLOSE 2910 (3 MPA.S), POLOXAMER 188, SACCHARIN SODIUM, WATER, XANTHAN GUM |
| Amneal Pharmaceuticals LLC 1 product | ||
| 750 mg/5 mL oral suspensionNDC 65162-0693-88 | Still being read | Not read yet |
| Atlantic Biologicals Corp. 2 products | ||
| 750 mg/5 mL oral suspensionNDC 17856-8631-01 | Benzyl alcohol Polyethylene glycol or polysorbate |
Show 6 ingredientsBENZYL ALCOHOL, HYPROMELLOSE 2910 (3 MPA.S), POLOXAMER 188, SACCHARIN SODIUM, WATER, XANTHAN GUM |
| 750 mg/5 mL oral suspensionNDC 17856-0631-01 | Still being read | Not read yet |
| AvKARE 1 product | ||
| 750 mg/5 mL oral suspensionNDC 73190-0098-21 | No inactive-ingredient list on the label | No list we could read |
| AvPAK 1 product | ||
| 750 mg/5 mL oral suspensionNDC 50268-0119-12 | Still being read | Not read yet |
| Bionpharma Inc. 1 product | ||
| 750 mg/5 mL oral suspensionNDC 69452-0252-87 | Benzyl alcohol Polyethylene glycol or polysorbate |
Show 7 ingredientsBENZYL ALCOHOL, HYDROCHLORIC ACID, POLOXAMER 188, SACCHARIN SODIUM, SODIUM HYDROXIDE, WATER, XANTHAN GUM |
| Camber Pharmaceuticals, Inc. 1 product | ||
| 750 mg/5 mL oral suspensionNDC 31722-0629-21 | Benzyl alcohol Polyethylene glycol or polysorbate |
Show 6 ingredientsBENZYL ALCOHOL, HYPROMELLOSE 2910 (3 MPA.S), POLOXAMER 188, SACCHARIN SODIUM, WATER, XANTHAN GUM |
| Chartwell Governmental & Specialty RX, LLC. 1 product | ||
| 750 mg/5 mL oral suspensionNDC 68999-0528-24 | Benzyl alcohol Polyethylene glycol or polysorbate |
Show 5 ingredientsBENZYL ALCOHOL, POLOXAMER 188, SACCHARIN SODIUM, WATER, XANTHAN GUM |
| Chartwell RX, LLC 1 product | ||
| 750 mg/5 mL oral suspensionNDC 62135-0528-09 | Still being read | Not read yet |
| GlaxoSmithKline LLC 2 products | ||
| 750 mg/5 mL oral suspensionNDC 00173-0547-00 | Benzyl alcohol Polyethylene glycol or polysorbate |
Show 5 ingredientsBENZYL ALCOHOL, POLOXAMER 188, SACCHARIN SODIUM, WATER, XANTHAN GUM |
| 750 mg/5 mL oral suspensionNDC 00173-0665-18 | Benzyl alcohol Polyethylene glycol or polysorbate |
Show 5 ingredientsBENZYL ALCOHOL, POLOXAMER 188, SACCHARIN SODIUM, WATER, XANTHAN GUM |
| Glenmark Pharmaceuticals Inc., USA 1 product | ||
| 750 mg/5 mL oral suspensionNDC 68462-0421-21 | Still being read | Not read yet |
| Golden State Medical Supply, Inc. 1 product | ||
| 750 mg/5 mL oral suspensionNDC 51407-0642-87 | Still being read | Not read yet |
| Kesin Pharma 1 product | ||
| 750 mg/5 mL oral suspensionNDC 81033-0104-22 | Still being read | Not read yet |
| Kesin Pharma Corporation 1 product | ||
| 750 mg/5 mL oral suspensionNDC 81033-0105-22 | Benzyl alcohol Polyethylene glycol or polysorbate |
Show 5 ingredientsBENZYL ALCOHOL, POLOXAMER 188, SACCHARIN SODIUM, WATER, XANTHAN GUM |
| KVK-Tech, Inc. 1 product | ||
| 750 mg/5 mL oral suspensionNDC 10702-0223-21 | Benzyl alcohol Polyethylene glycol or polysorbate |
Show 5 ingredientsBENZYL ALCOHOL, POLOXAMER 188, SACCHARIN SODIUM, WATER, XANTHAN GUM |
| Lupin Pharmaceuticals, Inc. 1 product | ||
| 750 mg/5 mL oral suspensionNDC 70748-0299-01 | Still being read | Not read yet |
| Major Pharmaceuticals 1 product | ||
| 750 mg/5 mL oral suspensionNDC 00904-7459-25 | Benzyl alcohol Polyethylene glycol or polysorbate |
Show 5 ingredientsBENZYL ALCOHOL, POLOXAMER 188, SACCHARIN SODIUM, WATER, XANTHAN GUM |
| NorthStar RxLLC 1 product | ||
| 750 mg/5 mL oral suspensionNDC 72603-0248-01 | Benzyl alcohol Polyethylene glycol or polysorbate |
Show 6 ingredientsBENZYL ALCOHOL, HYPROMELLOSE 2910 (3 MPA.S), POLOXAMER 188, SACCHARIN SODIUM, WATER, XANTHAN GUM |
| PAI Holdings, LLC dba PAI Pharma 2 products | ||
| 750 mg/5 mL oral suspensionNDC 00121-1016-18 | Benzyl alcohol Polyethylene glycol or polysorbate |
Show 5 ingredientsBENZYL ALCOHOL, HYPROMELLOSE 2910 (3 MPA.S), POLOXAMER 188, SACCHARIN SODIUM, XANTHAN GUM |
| 750 mg/5 mL oral suspensionNDC 00121-0956-08 | 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.
Atovaquone and benzyl alcohol
Benzyl alcohol: A preservative, mostly in injections and liquids; not for newborns. Every checked Atovaquone product (14) lists benzyl alcohol.
Lists benzyl alcohol
- A2A Integrated: 750 mg/5 mL oral suspension
- Abon: 750 mg/5 mL oral suspension
- American Health Packaging: 750 mg/5 mL oral suspension
- Atlantic Biologicals: 750 mg/5 mL oral suspension
- Bionpharma: 750 mg/5 mL oral suspension
- Camber: 750 mg/5 mL oral suspension
- Chartwell Governmental & Specialty RX: 750 mg/5 mL oral suspension
- GlaxoSmithKline: 750 mg/5 mL oral suspension (NDC 00173-0547-00), 750 mg/5 mL oral suspension (NDC 00173-0665-18)
- Kesin Pharma Corporation: 750 mg/5 mL oral suspension
- KVK-Tech: 750 mg/5 mL oral suspension
- Major: 750 mg/5 mL oral suspension
- NorthStar RxLLC: 750 mg/5 mL oral suspension
- PAI Holdings, LLC dba PAI: 750 mg/5 mL oral suspension
Atovaquone and polyethylene glycol or polysorbate
Polyethylene glycol or polysorbate: PEG, macrogol or polysorbate; a rare cause of allergic reactions. Every checked Atovaquone product (14) lists polyethylene glycol or polysorbate.
Lists polyethylene glycol or polysorbate
- A2A Integrated: 750 mg/5 mL oral suspension
- Abon: 750 mg/5 mL oral suspension
- American Health Packaging: 750 mg/5 mL oral suspension
- Atlantic Biologicals: 750 mg/5 mL oral suspension
- Bionpharma: 750 mg/5 mL oral suspension
- Camber: 750 mg/5 mL oral suspension
- Chartwell Governmental & Specialty RX: 750 mg/5 mL oral suspension
- GlaxoSmithKline: 750 mg/5 mL oral suspension (NDC 00173-0547-00), 750 mg/5 mL oral suspension (NDC 00173-0665-18)
- Kesin Pharma Corporation: 750 mg/5 mL oral suspension
- KVK-Tech: 750 mg/5 mL oral suspension
- Major: 750 mg/5 mL oral suspension
- NorthStar RxLLC: 750 mg/5 mL oral suspension
- PAI Holdings, LLC dba PAI: 750 mg/5 mL oral suspension
At the pharmacy counter
How to use this at the pharmacy counter
- 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.
- 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.
- 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.
- 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.
Common questions about Atovaquone inactive ingredients
Is Atovaquone gluten-free?
Does Atovaquone contain lactose?
Does Atovaquone contain soy?
Is there a dye-free Atovaquone?
Does Atovaquone contain gelatin?
Why do the inactive ingredients differ between manufacturers?
Can my pharmacy give me a specific manufacturer's version?
How current is this list?
Sources: the products are the finished Atovaquone 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 Atovaquone guide