Home NDC 81953-100 SCANTILY PAD
Product NDC 81953-100
11-digit product format 819530100
Labeler code 81953
Product ID 81953-100_48c4d99f-9b27-7bf3-e063-6394a90a57ee
Type HUMAN OTC DRUG
Nonproprietary name Acne Treatment
Dosage form LIQUID
Route TOPICAL
Labeler Dermala Inc
Application M006
Marketing category OTC MONOGRAPH DRUG
Marketing start 2021-06-01
Substance SALICYLIC ACID
Active strength .01 mg/mg
NDC exclude flag No
Listing certified through 2027-12-31
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 SCANTILY PAD
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SALICYLIC ACID .01 mg/mg
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.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 81953-100-01 SCANTILY PAD 50 mg in 1 JAR LIQUID 50 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 81953-100 SCANTILY PAD (ACNE TREATMENT) LIQUID [DERMALA INC] 5 Current NDC, Legacy NDC, 1 package rows 20241212_c5145f1d-78f7-22b4-e053-2a95a90a5c59.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.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 81953-100-01 81953010001 50 mg in 1 JAR (81953-100-01) 50 mg 2021-06-01 0000-00-00 No No Current