Home NDC 80176-002-03 ALLPURE HAND SANITIZER
Product NDC 80176-002
Requested package NDC 80176-002-03
11-digit product format 801760002
Labeler code 80176
Product ID 80176-002_d58d3756-8ee7-796f-e053-2995a90abb16
Type HUMAN OTC DRUG
Nonproprietary name Alcohol
Dosage form GEL
Route TOPICAL
Labeler CERCI KOZMETIK VE OTEL EKIPMANLARI PAZARLAMA IC VE DIS TICARET LIMITED SIRKETI
Application part333A
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2020-08-20
Marketing end 0000-00-00
Substance ALCOHOL
Active strength 70 mL/100mL
NDC exclude flag No
Listing certified through 2023-12-31
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.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 80176-002-01 ALLPURE HAND SANITIZER 30 mL in 1 BOTTLE, PLASTIC GEL 30 4 80176-002-02 ALLPURE HAND SANITIZER 50 mL in 1 BOTTLE, PLASTIC GEL 50 4 80176-002-03 ALLPURE HAND SANITIZER 100 mL in 1 BOTTLE, PLASTIC GEL 100 4 80176-002-04 ALLPURE HAND SANITIZER 250 mL in 1 BOTTLE, PLASTIC GEL 250 4 80176-002-05 ALLPURE HAND SANITIZER 500 mL in 1 BOTTLE, PLASTIC GEL 500 4 80176-002-06 ALLPURE HAND SANITIZER 1000 mL in 1 BOTTLE, PLASTIC GEL 1000 4 80176-002-07 ALLPURE HAND SANITIZER 5000 mL in 1 BOTTLE, PLASTIC GEL 5000 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 80176-002 ALLPURE HAND SANITIZER (ALCOHOL) GEL [CERCI KOZMETIK VE OTEL EKIPMANLARI PAZARLAMA IC VE DIS TICARET LIMITED SIRKETI] 4 Legacy NDC, 7 package rows 20231031_3fc927de-50c6-4bed-9595-a6559b6d1b04.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 80176-002-03 80176000203 100 mL in 1 BOTTLE, PLASTIC (80176-002-03) 100 ml 2020-08-20 0000-00-00 No No Current