Home NDC 58503-017-02 Instant Hand Sanitizer - Original
Product NDC 58503-017
Requested package NDC 58503-017-02
11-digit product format 585030017
Labeler code 58503
Product ID 58503-017_edb1a6e6-d7ff-3e5d-e053-2a95a90a5bda
Type HUMAN OTC DRUG
Nonproprietary name Ethyl Alcohol
Dosage form GEL
Route TOPICAL
Labeler China Ningbo Shangge Cosmetic Technology Corp.
Application part333E
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2013-07-05
Marketing end 0000-00-00
Substance ALCOHOL
Active strength 33 mL/53mL
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.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 58503-017-01 Instant Hand Sanitizer - Original 53 mL in 1 BOTTLE GEL 53 3 58503-017-02 Instant Hand Sanitizer - Original 2 in 1 PACKAGE GEL 2 3
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 58503-017 INSTANT HAND SANITIZER - ORIGINAL (ETHYL ALCOHOL) GEL [CHINA NINGBO SHANGGE COSMETIC TECHNOLOGY CORP.] 3 Legacy NDC, 2 package rows 20221118_74b3da8c-efff-4a96-867a-d7aa258502b2.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 58503-017-02 58503001702 2 BOTTLE in 1 PACKAGE (58503-017-02) > 53 mL in 1 BOTTLE (58503-017-01) 2 bottle 2013-07-05 0000-00-00 No No Current