Home NDC 59088-214 Salicate
Product NDC 59088-214
11-digit product format 590880214
Labeler code 59088
Product ID 59088-214_fd699cfb-8ca0-ebb8-e053-6394a90ace4a
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Salicylic Acid 10%
Dosage form GEL
Route TOPICAL
Labeler PureTek Coproration
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2023-10-13
Substance SALICYLIC ACID
Active strength 10 mg/100mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes 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 Salicate
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SALICYLIC ACID 10 mg/100mL
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 59088-214-03 Salicate 30 mL in 1 BOTTLE, DROPPER GEL 30 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 59088-214 SALICATE (SALICYLIC ACID 10%) GEL [PURETEK COPRORATION] 1 Current NDC, 1 package rows 20231014_fd699cfb-8c9f-ebb8-e053-6394a90ace4a.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 1 of 1 · 1 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Salicate SALICYLIC ACID 10% PureTek Coproration fd699cfb-8c9f-ebb8-e053-6394a90ace4a 2023-10-13 Warnings, Adverse reactions Exact identifier ndc (product): 59088-214
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 59088-214-03 59088021403 30 mL in 1 BOTTLE, DROPPER (59088-214-03) 30 ml 2023-10-13 No No Current