Home NDC 51142-444 Alcohol Prep Pad
Product NDC 51142-444
11-digit product format 511420444
Labeler code 51142
Product ID 51142-444_25da293c-7ff5-8fe3-e063-6394a90a9af1
Type HUMAN OTC DRUG
Nonproprietary name Alcohol Prep Pad
Dosage form LIQUID
Route TOPICAL
Labeler ASO LLC
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2018-09-24
Substance ISOPROPYL ALCOHOL
Active strength 70 mL/100mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Alcohol Prep Pad
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ISOPROPYL ALCOHOL 70 mL/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination ND2M416302 Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 51142-444-01 Alcohol Prep Pad 0.4 mL in 1 POUCH LIQUID 0.4 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 51142-444 ALCOHOL PREP PAD LIQUID [ASO LLC] 4 Current NDC, Legacy NDC, 1 package rows 20241103_7481bfb9-2baf-b1ec-e053-2991aa0ad2de.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 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 51142-444-01 51142044401 .4 mL in 1 POUCH (51142-444-01) 2018-09-24 0000-00-00 No No Current