Home NDC 41250-370-06 Advanced Hand Sanitizer
Product NDC 41250-370
Requested package NDC 41250-370-06
11-digit product format 412500370
Labeler code 41250
Product ID 41250-370_4b33a939-c22a-ff10-e063-6294a90adca5
Type HUMAN OTC DRUG
Nonproprietary name Ethyl alcohol
Dosage form GEL
Route TOPICAL
Labeler Meijer, Inc.
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 1992-04-24
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 · 1 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 41250-370 41250-370-06 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…
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 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 41250-370-06 Advanced Hand Sanitizer 33 mL in 1 BOTTLE, PLASTIC GEL 33 20 41250-370-16 Advanced Hand Sanitizer 59 mL in 1 BOTTLE, PLASTIC GEL 59 20 41250-370-34 Advanced Hand Sanitizer 236 mL in 1 BOTTLE, PUMP GEL 236 20 41250-370-45 Advanced Hand Sanitizer 946 mL in 1 BOTTLE, PLASTIC GEL 946 20
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded ALCOHOL ACTIVE INGREDIENT 3K9958V90M ADVANCED HAND SANITIZER (ETHYL ALCOHOL) GEL [MEIJER DISTRIBUTION, INC] 2 ALCOHOL ACTIVE MOIETY 3K9958V90M ADVANCED HAND SANITIZER (ETHYL ALCOHOL) GEL [MEIJER DISTRIBUTION, INC] 2 .ALPHA.-TOCOPHEROL ACETATE INACTIVE INGREDIENT 9E8X80D2L0 ADVANCED HAND SANITIZER (ETHYL ALCOHOL) GEL [MEIJER DISTRIBUTION, INC] 2 CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) INACTIVE INGREDIENT 71DD5V995L ADVANCED HAND SANITIZER (ETHYL ALCOHOL) GEL [MEIJER DISTRIBUTION, INC] 2 GLYCERIN INACTIVE INGREDIENT PDC6A3C0OX ADVANCED HAND SANITIZER (ETHYL ALCOHOL) GEL [MEIJER DISTRIBUTION, INC] 2 GLYCERYL CAPRYLATE/CAPRATE INACTIVE INGREDIENT G7515SW10N ADVANCED HAND SANITIZER (ETHYL ALCOHOL) GEL [MEIJER DISTRIBUTION, INC] 2 ISOPROPYL MYRISTATE INACTIVE INGREDIENT 0RE8K4LNJS ADVANCED HAND SANITIZER (ETHYL ALCOHOL) GEL [MEIJER DISTRIBUTION, INC] 2 SULISOBENZONE INACTIVE INGREDIENT 1W6L629B4K ADVANCED HAND SANITIZER (ETHYL ALCOHOL) GEL [MEIJER DISTRIBUTION, INC] 2 water INACTIVE INGREDIENT 059QF0KO0R ADVANCED HAND SANITIZER (ETHYL ALCOHOL) GEL [MEIJER DISTRIBUTION, INC] 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 41250-370 ADVANCED HAND SANITIZER (ETHYL ALCOHOL) GEL [MEIJER DISTRIBUTION, INC] 18 Current NDC, Legacy NDC, 4 package rows 20240820_a56b4a66-3923-4e40-a461-1d97043fb89a.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 41250-370-06 41250037006 33 mL in 1 BOTTLE, PLASTIC (41250-370-06) 33 ml 1992-04-24 0000-00-00 No No Current