Home NDC 77720-016-01 CLEANZE HAND SANITIZING
Product NDC 77720-016
Requested package NDC 77720-016-01
11-digit product format 777200016
Labeler code 77720
Product ID 77720-016_b7e2e277-352f-edb9-e053-2995a90aaf2a
Type HUMAN OTC DRUG
Nonproprietary name ethyl alcohol
Dosage form GEL
Route TOPICAL
Labeler Skaffles Group Limited Liability Company
Application part333A
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2020-12-30
Marketing end 0000-00-00
Substance ALCOHOL
Active strength 71 mL/100mL
NDC exclude flag No
Listing certified through 2022-12-31
Current FDA listing Historical FDA.report record 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 · 9 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Code, Status table Captured / source date Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 77720-016-01 CLEANZE HAND SANITIZING 500 mL in 1 BOTTLE GEL 500 1 77720-016-02 CLEANZE HAND SANITIZING 1000 mL in 1 BOTTLE GEL 1000 1 77720-016-03 CLEANZE HAND SANITIZING 237 mL in 1 BOTTLE GEL 237 1 77720-016-04 CLEANZE HAND SANITIZING 60 mL in 1 BOTTLE GEL 60 1 77720-016-05 CLEANZE HAND SANITIZING 100 mL in 1 BOTTLE GEL 100 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 77720-016 CLEANZE HAND SANITIZING (ETHYL ALCOHOL) GEL [SKAFFLES GROUP LIMITED LIABILITY COMPANY] 1 Legacy NDC, 5 package rows 20210102_b7e2e993-05f3-e992-e053-2995a90aa188.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 77720-016-01 77720001601 500 mL in 1 BOTTLE (77720-016-01) 500 ml 2020-12-30 0000-00-00 No No Current