Home NDC 69540-0025-2 Clorox Hand Sanitizer
Product NDC 69540-0025
Requested package NDC 69540-0025-2
11-digit product format 695400025
Labeler code 69540
Product ID 69540-0025_2f6a3062-891e-971d-e063-6394a90a8536
Type HUMAN OTC DRUG
Nonproprietary name ALCOHOL
Dosage form GEL
Route TOPICAL
Labeler Brand Buzz LLC
Application M003
Marketing category OTC MONOGRAPH DRUG
Marketing start 2021-03-19
Substance ALCOHOL
Active strength 71 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 · 3 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 2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 69540-0025 69540-0025-2 U Excluded because listing certification expired excluded / ndc_excluded.zip 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 69540-0025 69540-0025-2 U Excluded because listing certification expired excluded / ndc_excluded.zip ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 69540-0025 69540-0025-2 U Excluded because listing certification expired excluded / ndc_excluded.zip 0efc9e666f02…f202fb6c5f17…
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 Clorox Hand Sanitizer
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALCOHOL 71 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 2282911 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 69540-0025-1 Clorox Hand Sanitizer 100 in 1 BOX GEL 100 3 69540-0025-1 Clorox Hand Sanitizer 2 mL in 1 PACKET GEL 2 3 69540-0025-2 Clorox Hand Sanitizer 500 mL in 1 BOTTLE GEL 500 3 69540-0025-3 Clorox Hand Sanitizer 1000 mL in 1 BOTTLE GEL 1000 3 69540-0025-4 Clorox Hand Sanitizer 1000 mL in 1 BOTTLE GEL 1000 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69540-0025 CLOROX HAND SANITIZER (ALCOHOL) GEL [BRAND BUZZ LLC] 3 Current NDC, Legacy NDC, 5 package rows 20250305_bdd47d2f-5332-1430-e053-2a95a90a1c33.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 9 of 115 · 2,286 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 69540-0025-2 69540002502 500 mL in 1 BOTTLE (69540-0025-2) 500 ml 2021-03-19 0000-00-00 No No Current