Home NDC 50718-0032 Clear Acne Spot Treatment
Product NDC 50718-0032
11-digit product format 507180032
Labeler code 50718
Product ID 50718-0032_d8bfce91-7eeb-4696-ae5f-b4fa7514f928
Type HUMAN OTC DRUG
Nonproprietary name Acne Spot Treatment
Dosage form LIQUID
Route TOPICAL
Labeler Kamedis
Application M006
Marketing category OTC MONOGRAPH DRUG
Marketing start 2018-01-01
Substance SALICYLIC ACID
Active strength 28.8 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 Clear Acne Spot Treatment
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SALICYLIC ACID 28.8 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 SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 50718-0032-1 Clear Acne Spot Treatment 1 in 1 CARTON LIQUID 1 5 50718-0032-1 Clear Acne Spot Treatment 22 mL in 1 BOTTLE LIQUID 22 5 50718-0032-1 Clear Acne Kit 1 in 1 CARTON LIQUID 28.8 mg in 1mL 2 50718-0032-1 Clear Acne Kit 22 mL in 1 BOTTLE LIQUID 22 mL 28.8 mg in 1mL 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 50718-0032 CLEAR ACNE SPOT TREATMENT (ACNE SPOT TREATMENT) LIQUID [KAMEDIS] 5 Current NDC, Legacy NDC, 2 package rows 20240214_00764a10-f1fe-45f5-89b4-9e891a221004.zip 50718-0032 CLEAR ACNE KIT (ACNE KIT) KIT [KAMEDIS] 2 Current NDC, Legacy NDC 20200708_de311f9e-a8e6-4a3e-ada0-b3882bb67b6c.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 50 of 54 · 1,077 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 50718-0032-1 50718003201 1 BOTTLE in 1 CARTON (50718-0032-1) / 22 mL in 1 BOTTLE 1 bottle 2018-01-01 0000-00-00 No No Current