Home NDC 73670-606 NAELI Exfoliator AHA-BHA Face Cleanser
Product NDC 73670-606
11-digit product format 736700606
Labeler code 73670
Product ID 73670-606_35b6571b-130f-cf57-e063-6294a90aae80
Type HUMAN OTC DRUG
Nonproprietary name SALICYLIC ACID
Dosage form GEL
Route TOPICAL
Labeler ALLI LLC
Application M006
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-05-07
Substance SALICYLIC ACID
Active strength 10 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 NAELI Exfoliator AHA-BHA Face Cleanser
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SALICYLIC ACID 10 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 1038982 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 73670-606-00 NAELI Exfoliator AHA-BHA Face Cleanser 177 mL in 1 BOTTLE GEL 177 1 73670-606-00 NAELI Exfoliator AHA-BHA Face Cleanser 1 in 1 BOX GEL 1 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 73670-606 NAELI EXFOLIATOR AHA-BHA FACE CLEANSER (SALICYLIC ACID) GEL [ALLI LLC] 1 Current NDC, 2 package rows 20250523_16bf50c6-4a9d-4242-94a2-d2165b82e7ce.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 73670-606-00 73670060600 1 BOTTLE in 1 BOX (73670-606-00) / 177 mL in 1 BOTTLE 1 bottle 2025-05-07 No No Current