Home NDC 11673-439 Advanced Hand Sanitizer
Product NDC 11673-439
11-digit product format 116730439
Labeler code 11673
Product ID 11673-439_4b1e9776-8205-7c23-e063-6394a90a78f6
Type HUMAN OTC DRUG
Nonproprietary name Ethyl Alcohol
Dosage form GEL
Route TOPICAL
Labeler Target Corporation
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2012-12-13
Substance ALCOHOL
Active strength 70 mL/100mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 24 matching rows.
View current auxiliary records. · View the auxiliary file history.
Additional Listing Data#
Finished product Yes
Brand name base Advanced Hand Sanitizer
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 RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 581662 Internal RxNorm 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 11673-439-16 Advanced Hand Sanitizer 59 mL in 1 BOTTLE, DISPENSING GEL 59 17 11673-439-34 Advanced Hand Sanitizer 236 mL in 1 BOTTLE, DISPENSING GEL 236 17 11673-439-45 Advanced Hand Sanitizer 946 mL in 1 BOTTLE, DISPENSING GEL 946 17
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 11673-439 ADVANCED HAND SANITIZER (ETHYL ALCOHOL) GEL [TARGET CORP] 15 Current NDC, Legacy NDC, 3 package rows 20240221_e877e196-fa56-42e2-8b32-4509b1be8575.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 Marketing end Sample Exclude flag Status 11673-439-16 11673043916 59 mL in 1 BOTTLE, DISPENSING (11673-439-16) 59 ml 2012-12-13 0000-00-00 No No Current 11673-439-34 11673043934 236 mL in 1 BOTTLE, DISPENSING (11673-439-34) 236 ml 2012-12-13 0000-00-00 No No Current 11673-439-45 11673043945 946 mL in 1 BOTTLE, DISPENSING (11673-439-45) 946 ml 2012-12-13 0000-00-00 No No Current