Home NDC 71220-088 innisfree Gentle Retinol Salicylic Acne Serum
Product NDC 71220-088
11-digit product format 712200088
Labeler code 71220
Product ID 71220-088_2b38c5cc-cb91-3168-e063-6294a90a5abc
Type HUMAN OTC DRUG
Nonproprietary name Salicylic Acid Gel
Dosage form GEL
Route TOPICAL
Labeler Innisfree Corporation
Application M006
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-03-01
Substance SALICYLIC ACID
Active strength 1 g/50mL
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 innisfree Gentle Retinol Salicylic Acne Serum
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SALICYLIC ACID 1 g/50mL
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 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 346298 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 71220-088-02 innisfree Gentle Retinol Salicylic Acne Serum 1 in 1 BOX GEL 1 1 71220-088-02 innisfree Gentle Retinol Salicylic Acne Serum 30 mL in 1 TUBE GEL 30 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71220-088 INNISFREE GENTLE RETINOL SALICYLIC ACNE SERUM (SALICYLIC ACID GEL) GEL [INNISFREE CORPORATION] 1 Current NDC, 2 package rows 20250302_2b38b6f2-0de5-581b-e063-6394a90acd55.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 7 of 55 · 1,088 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 71220-088-02 71220008802 1 TUBE in 1 BOX (71220-088-02) / 30 mL in 1 TUBE 1 tube 2025-03-01 No No Current