Home NDC 71734-309-02 Antibacterial Hand Sanitizer
Product NDC 71734-309
Requested package NDC 71734-309-02
11-digit product format 717340309
Labeler code 71734
Product ID 71734-309_adc34e95-4a47-476d-bc1d-e25779fba04f
Type HUMAN OTC DRUG
Nonproprietary name Alcohol
Dosage form GEL
Route TOPICAL
Labeler JIANGMEN SHUIZIRUN SANITARY ARTICLES CO., LTD.
Application part333E
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2020-05-02
Marketing end 0000-00-00
Substance ALCOHOL
Active strength 62 mL/100mL
NDC exclude flag No
Listing certified through 2021-12-31
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 71734-309-01 Antibacterial Hand Sanitizer 54 mL in 1 BOTTLE GEL 54 1 71734-309-02 Antibacterial Hand Sanitizer 60 mL in 1 BOTTLE GEL 60 1 71734-309-03 Antibacterial Hand Sanitizer 100 mL in 1 BOTTLE GEL 100 1 71734-309-04 Antibacterial Hand Sanitizer 238 mL in 1 BOTTLE GEL 238 1 71734-309-05 Antibacterial Hand Sanitizer 500 mL in 1 BOTTLE GEL 500 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71734-309 ANTIBACTERIAL HAND SANITIZER (ALCOHOL) GEL [JIANGMEN SHUIZIRUN SANITARY ARTICLES CO., LTD.] 1 Legacy NDC, 5 package rows 20200502_43352be2-1077-443d-a264-1a834f692996.zip
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 71734-309-02 71734030902 60 mL in 1 BOTTLE (71734-309-02) 60 ml 2020-05-02 0000-00-00 No No Current