Home NDC 59899-002 enfuselle Acne Clarifying
Product NDC 59899-002
11-digit product format 598990002
Labeler code 59899
Product ID 59899-002_09495cdc-6fd1-9f95-e063-6394a90a7d5c
Type HUMAN OTC DRUG
Nonproprietary name SALICYLIC ACID
Dosage form LOTION
Route TOPICAL
Labeler Shaklee Corporation
Application M006
Marketing category OTC MONOGRAPH DRUG
Marketing start 2013-08-08
Substance SALICYLIC ACID
Active strength 5 mg/mL
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 enfuselle Acne Clarifying
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SALICYLIC ACID 5 mg/mL
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 199134 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 59899-002-01 enfuselle Acne Clarifying 29 mL in 1 TUBE LOTION 29 10 59899-002-01 enfuselle Acne Clarifying 1 in 1 CARTON LOTION 1 10
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 59899-002 ENFUSELLE ACNE CLARIFYING (SALICYLIC ACID) LOTION [SHAKLEE CORPORATION] 10 Current NDC, Legacy NDC, 2 package rows 20231104_dd429a9b-5c2d-4310-8506-6487b02e3880.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 40 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 Marketing end Sample Exclude flag Status 59899-002-01 59899000201 1 TUBE in 1 CARTON (59899-002-01) / 29 mL in 1 TUBE 1 tube 2013-08-08 0000-00-00 No No Current