Home NDC 57337-120 Hand Sanitizer Antibacterial
Product NDC 57337-120
11-digit product format 573370120
Labeler code 57337
Product ID 57337-120_2e0157b2-9e7a-93b1-e063-6294a90a6062
Type HUMAN OTC DRUG
Nonproprietary name Ethyl Alcohol
Dosage form LIQUID
Route TOPICAL
Labeler Ningbo Rejoice International
Application M003
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-03-05
Substance ALCOHOL
Active strength 70 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 · 9 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2025-02-02 03:52 UTC · source 2025-01-31 excluded product product 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 57337-120-01 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 57337-120-02 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 57337-120-01 ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 57337-120-02 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 57337-120-01 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 57337-120-02 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 Hand Sanitizer Antibacterial
Brand name suffix Vitamin E
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALCOHOL 70 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 582753 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 57337-120-01 Hand Sanitizer AntibacterialVitamin E 500 mL in 1 BOTTLE LIQUID 500 3 57337-120-02 Hand Sanitizer AntibacterialVitamin E 177 mL in 1 BOTTLE LIQUID 177 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 57337-120 HAND SANITIZER ANTIBACTERIAL VITAMIN E (ETHYL ALCOHOL) LIQUID [NINGBO REJOICE INTERNATIONAL] 3 Current NDC, Legacy NDC, 2 package rows 20250215_a346ebd2-fc31-b574-e053-2995a90a0d3a.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 70 of 114 · 2,277 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 57337-120-01 57337012001 500 mL in 1 BOTTLE (57337-120-01) 500 ml 2020-04-14 0000-00-00 No No Current 57337-120-02 57337012002 177 mL in 1 BOTTLE (57337-120-02) 177 ml 2020-03-05 0000-00-00 No No Current