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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82442-031-02Ethanol59 mL in 1 BOTTLE, PLASTICGEL593

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82442-031ETHANOL (ALCOHOL) GEL [TARGET CORPORATION INC.]2Current NDC, 1 package rows20250322_28ef35a8-e6ca-9669-e063-6394a90abf8f.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
82442-031-028244200310259 mL in 1 BOTTLE, PLASTIC (82442-031-02) 59 ml2025-03-01NoNoHistorical