Home NDC 82442-031 Ethanol
Product NDC 82442-031
11-digit product format 824420031
Labeler code 82442
Product ID 82442-031_50f05b46-2822-f937-e063-6294a90addfc
Type HUMAN OTC DRUG
Nonproprietary name Alcohol
Dosage form GEL
Route TOPICAL
Labeler TARGET CORPORATION INC.
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-03-01
Substance ALCOHOL
Active strength 70 mL/100mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Ethanol
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength 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 3K9958V90M Internal UNII 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 82442-031-02 Ethanol 59 mL in 1 BOTTLE, PLASTIC GEL 59 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 82442-031 ETHANOL (ALCOHOL) GEL [TARGET CORPORATION INC.] 2 Current NDC, 1 package rows 20250322_28ef35a8-e6ca-9669-e063-6394a90abf8f.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 Units Marketing start Sample Exclude flag Status 82442-031-02 82442003102 59 mL in 1 BOTTLE, PLASTIC (82442-031-02) 59 ml 2025-03-01 No No Current