Salicylic Acid
Liquid Wart Remover
- Strength
- .17 g/9mL
- Form
- Liquid
Chain Drug Marketing Association Inc.
Compare any two to four medications side by side — what is actually in them, how strong they are, how they are taken and who makes them. Built on the 112,035 products in the US FDA National Drug Code directory.
1,437 medications
Tick up to 4 to compare.
Liquid Wart Remover
Chain Drug Marketing Association Inc.
Medicated Corn Removers
VALU MERCHANDISERS, CO
Medicated Callus Removers
VALU MERCHANDISERS, CO
Corn and Callus Remover Kit
VALU MERCHANDISERS, CO
Liquid Wart Remover
VALU MERCHANDISERS, CO
Medicated Callus Removers Extra Thick
VALU MERCHANDISERS, CO
Wart Remover Gel Tube
VALU MERCHANDISERS, CO
Medicated Corn Removers
Harris Teeter, LLC
Medicated Callus Removers
Harris Teeter, LLC
Wart Remover Liquid
Harris Teeter, LLC
Liquid Corn and Callus Remover
Harris Teeter, LLC
Gel Corn Remover
CVS Pharmacy
Liquid Wart Remover
LEADER/ Cardinal Health 110, Inc.
Medicated Corn Removers
LEADER/ Cardinal Health 110, Inc.
Liquid Corn and Callus Remover
LEADER/ Cardinal Health 110, Inc.
Medicated Callus Removers
LEADER/ Cardinal Health 110, Inc.
D3 Development, Inc.
Medicated Corn Removers
Hudson Health LLC
Medicated Corn Removers
Hudson Health LLC
Liquid Wart Remover
Hudson Health LLC
Corn and Callus Remover Kit
Hudson Health LLC
Medicated Plantar Wart Remover
Hudson Health LLC
Topco Associates LLC
Corn and Callus Remover Kit
Wal-Mart Stores, Inc.
Most medications exist under several names: one brand name, one generic name, and a different brand again in another country. What matters is the active ingredient and its strength — two products with the same ingredient at the same strength are, for most purposes, the same medicine.
A 10 mg tablet is not "better" than a 5 mg one. Strength is matched to the person and the condition, and a higher one is not an upgrade. Only your prescriber can say which is right for you.
The same ingredient as a tablet, a capsule or a liquid can be absorbed at different speeds. Modified-release forms in particular are not interchangeable with ordinary ones, even at an identical stated strength.
NDA is an original brand-name approval. ANDA is a generic, which had to prove it delivers the ingredient to the bloodstream at a rate and extent statistically equivalent to the original. OTC monograph covers products sold without a prescription under standing FDA rules.
A DEA schedule badge means the medication is federally controlled because of its potential for dependence or misuse. Schedule II is the most tightly restricted of those available by prescription. These carry extra rules on prescribing, refills and supply.
Where we stock a product containing the same active ingredient, the card says so and links to it. That is an ingredient match — the strength, form or manufacturer of what we sell may differ from the FDA record shown, so check the product page before ordering.
This tool is for information only and is not medical advice. It cannot tell you whether a medication is safe or suitable for you, and nothing here replaces a conversation with a prescriber or pharmacist. Source data is published by the U.S. Food & Drug Administration via openFDA and is reproduced without their endorsement; the FDA states it should not be relied upon for decisions about medical care.
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