Home NDC 59779-500 Salicylic Acid
Product NDC 59779-500
11-digit product format 597790500
Labeler code 59779
Product ID 59779-500_50b5089e-0007-a149-e063-6294a90a5bd2
Type HUMAN OTC DRUG
Nonproprietary name Wart Remover Liquid
Dosage form LIQUID
Route TOPICAL
Labeler CVS Pharmacy
Application M028
Marketing category OTC MONOGRAPH DRUG
Marketing start 2014-01-01
Substance SALICYLIC ACID
Active strength .17 mg/15mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 9 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Salicylic Acid
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SALICYLIC ACID .17 mg/15mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination O414PZ4LPZ Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 59779-500-09 Salicylic Acid 9 mL in 1 BOTTLE, WITH APPLICATOR LIQUID 9 18 59779-500-15 Salicylic Acid 15 mL in 1 BOTTLE, WITH APPLICATOR LIQUID 15 18
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 59779-500 SALICYLIC ACID (WART REMOVER LIQUID) LIQUID [CVS PHARMACY] 14 Current NDC, Legacy NDC, 2 package rows 20241228_90bc4d32-f865-4e33-86a0-4b860b610fa8.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 16 of 16 · 305 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 59779-500-09 59779050009 9 mL in 1 BOTTLE, WITH APPLICATOR (59779-500-09) 9 ml 2015-05-01 0000-00-00 No No Current 59779-500-15 59779050015 15 mL in 1 BOTTLE, WITH APPLICATOR (59779-500-15) 15 ml 2014-01-01 0000-00-00 No No Current