United States · FDA National Drug Code directory
Salicylic Acid
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 50804-749_40abb5bf-39a0-881b-e063-6394a90af13a
- Product NDC
- 50804-749
- Form
- LIQUID
- Composition / generic term
- Corn and Callus Remover
- Labeler
- Geiss, Destin & Dunn, Inc.
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20150810
- Source listing expiry
- 20261231
Source-listed ingredients
- SALICYLIC ACID — .17 g/9.8mL
These values do not establish equivalence or a dose recommendation.
Packages
- 9.8 mL in 1 BOTTLE, WITH APPLICATOR (50804-749-03) · 50804-749-03
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →