Home NDC 82442-003-08 Alcohol
Product NDC 82442-003
Requested package NDC 82442-003-08
11-digit product format 824420003
Labeler code 82442
Product ID 82442-003_5c437b61-7159-240a-e063-6294a90acc32
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 2024-03-01
Substance ALCOHOL
Active strength 70 mL/100mL
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 Alcohol
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALCOHOL 70 mL/100mL
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 82442-003-02 Alcohol 59 mL in 1 BOTTLE, PLASTIC GEL 59 5 82442-003-08 Alcohol 236 mL in 1 BOTTLE, PLASTIC GEL 236 5 82442-003-32 Alcohol 946 mL in 1 BOTTLE, PLASTIC GEL 946 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 82442-003 ALCOHOL GEL [TARGET CORPORATION INC.] 3 Current NDC, 3 package rows 20240816_092f6934-d697-2104-e063-6294a90a0b32.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.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 82442-003-08 82442000308 236 mL in 1 BOTTLE, PLASTIC (82442-003-08) 236 ml 2024-03-01 No No Current