Home NDC 30142-596 Hand Sanitizer
Product NDC 30142-596
11-digit product format 301420596
Labeler code 30142
Product ID 30142-596_4bd13d98-26c0-5f29-e063-6294a90a61da
Type HUMAN OTC DRUG
Nonproprietary name Ethyl alcohol
Dosage form GEL
Route TOPICAL
Labeler The Kroger Co.
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2012-09-17
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 · 2 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 30142-596 30142-596-34 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 30142-596 30142-596-45 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 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 30142-596-16 Hand Sanitizer 59 mL in 1 BOTTLE, PLASTIC GEL 59 16 30142-596-34 Hand Sanitizer 236 mL in 1 BOTTLE, PLASTIC GEL 236 16 30142-596-45 Hand Sanitizer 945 mL in 1 BOTTLE, PLASTIC GEL 945 16
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 30142-596 HAND SANITIZER (ETHYL ALCOHOL) GEL [THE KROGER CO] 14 Current NDC, Legacy NDC, 3 package rows 20240913_9f95d956-25db-4ffa-86cc-a160677124b8.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 30142-596-16 30142059616 59 mL in 1 BOTTLE, PLASTIC (30142-596-16) 59 ml 2012-09-17 0000-00-00 No No Current 30142-596-34 30142059634 236 mL in 1 BOTTLE, PLASTIC (30142-596-34) 236 ml 2012-09-17 0000-00-00 No No Current 30142-596-45 30142059645 945 mL in 1 BOTTLE, PLASTIC (30142-596-45) 945 ml 2012-09-17 0000-00-00 No No Current