Home NDC 62742-4076 DermaClear Pads
Product NDC 62742-4076
11-digit product format 627424076
Labeler code 62742
Product ID 62742-4076_288e4011-61f3-279d-e063-6394a90a7b00
Type HUMAN OTC DRUG
Nonproprietary name Salicylic Acid
Dosage form LIQUID
Route TOPICAL
Labeler Allure Labs
Application M006
Marketing category OTC MONOGRAPH DRUG
Marketing start 2015-05-08
Substance SALICYLIC ACID
Active strength 20 mg/g
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 4 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Code Status Snapshot Source SHA-256 2020-06-10 20:45 UTC · source 2020-06-10 excluded product product I Inactivated by FDA 9bebd1f3094a…5416666fcb17…2020-06-10 20:45 UTC · source 2020-06-10 excluded package package 62742-4076-1 I Inactivated by FDA 9bebd1f3094a…5416666fcb17…2019-12-08 06:16 UTC · source 2019-12-05 excluded product product E Excluded after deficient or non-compliant submission was not corrected 110d247fa046…a55b01930146…2019-12-08 06:16 UTC · source 2019-12-05 excluded package package 62742-4076-1 E Excluded after deficient or non-compliant submission was not corrected 110d247fa046…a55b01930146…
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 DermaClear Pads
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SALICYLIC ACID 20 mg/g
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 797892 Internal RxNorm 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 62742-4076-1 DermaClear Pads 85 g in 1 JAR LIQUID 85 3 62742-4076-2 DermaClear Pads 1 in 1 CARTON LIQUID 1 3
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded SALICYLIC ACID ACTIVE INGREDIENT O414PZ4LPZ DERMACLEAR PADS (SALICYLIC ACID) LIQUID [ALLURE LABS, INC] 1 SALICYLIC ACID ACTIVE MOIETY O414PZ4LPZ DERMACLEAR PADS (SALICYLIC ACID) LIQUID [ALLURE LABS, INC] 1 ALCOHOL INACTIVE INGREDIENT 3K9958V90M DERMACLEAR PADS (SALICYLIC ACID) LIQUID [ALLURE LABS, INC] 1 ALLANTOIN INACTIVE INGREDIENT 344S277G0Z DERMACLEAR PADS (SALICYLIC ACID) LIQUID [ALLURE LABS, INC] 1 ALOE VERA LEAF INACTIVE INGREDIENT ZY81Z83H0X DERMACLEAR PADS (SALICYLIC ACID) LIQUID [ALLURE LABS, INC] 1 AMMONIA INACTIVE INGREDIENT 5138Q19F1X DERMACLEAR PADS (SALICYLIC ACID) LIQUID [ALLURE LABS, INC] 1 GLYCERIN INACTIVE INGREDIENT PDC6A3C0OX DERMACLEAR PADS (SALICYLIC ACID) LIQUID [ALLURE LABS, INC] 1 GLYCOLIC ACID INACTIVE INGREDIENT 0WT12SX38S DERMACLEAR PADS (SALICYLIC ACID) LIQUID [ALLURE LABS, INC] 1 PEG-8/SMDI COPOLYMER INACTIVE INGREDIENT CCX72L6NY6 DERMACLEAR PADS (SALICYLIC ACID) LIQUID [ALLURE LABS, INC] 1 TEA TREE OIL INACTIVE INGREDIENT VIF565UC2G DERMACLEAR PADS (SALICYLIC ACID) LIQUID [ALLURE LABS, INC] 1 WATER INACTIVE INGREDIENT 059QF0KO0R DERMACLEAR PADS (SALICYLIC ACID) LIQUID [ALLURE LABS, INC] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 62742-4076 DERMACLEAR PADS (SALICYLIC ACID) LIQUID [ALLURE LABS] 3 Current NDC, Legacy NDC, 2 package rows 20241208_0c6624fd-88f9-402c-8ac2-bc278242b484.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 8 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 62742-4076-1 62742407601 85 g in 1 JAR 85 g Historical 62742-4076-2 62742407602 1 JAR in 1 CARTON (62742-4076-2) / 85 g in 1 JAR (62742-4076-1) 1 jar 2015-05-08 0000-00-00 No No Current