Home NDC 51142-595 Compound W
Product NDC 51142-595
11-digit product format 511420595
Labeler code 51142
Product ID 51142-595_52ccbaf1-bf0c-4adc-e063-6294a90ac8cc
Type HUMAN OTC DRUG
Nonproprietary name Salicylic acid gel
Dosage form GEL
Route TOPICAL
Labeler ASO LLC
Application M028
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-12-01
Marketing end 2029-02-20
Substance SALICYLIC ACID
Active strength 170 mg/g
NDC exclude flag No
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 · 2 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2022-08-30 03:57 UTC · source 2022-08-29 excluded product product 51142-595 I Inactivated by FDA excluded / ndc_excluded.zip fb8cb913e6d1…eb8c232b6be0…2022-08-30 03:57 UTC · source 2022-08-29 excluded package package 51142-595 51142-595-12 I Inactivated by FDA excluded / ndc_excluded.zip fb8cb913e6d1…eb8c232b6be0…
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 Compound W Active Ingredients# Ingredient, Strength table Ingredient Strength SALICYLIC ACID 170 mg/g
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 RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 210140 Internal RxNorm lookup 312880 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 51142-595-12 Compound W 7 g in 1 TUBE GEL 7 5 51142-595-12 Compound W 1 in 1 CARTON GEL 1 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 51142-595 COMPOUND W (SALICYLIC ACID GEL) GEL [ASO LLC] 4 Current NDC, Legacy NDC, 2 package rows 20231116_b55c7421-a8fe-8d4e-e053-2a95a90a7a6f.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.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 51142-595-12 51142059512 1 TUBE in 1 CARTON (51142-595-12) / 7 g in 1 TUBE 1 tube 2020-12-01 2029-02-20 No No Current