Home NDC 51801-779-08 Amcon Labs Hand Sanitizer Light Cleansing
Product NDC 51801-779
Requested package NDC 51801-779-08
11-digit product format 518010779
Labeler code 51801
Product ID 51801-779_5c529173-2cde-0688-e063-6294a90a615c
Type HUMAN OTC DRUG
Nonproprietary name Alcohol
Dosage form SPRAY
Route TOPICAL
Labeler Nomax, Inc.
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-08-04
Substance ALCOHOL
Active strength 600 mL/L
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes 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 Amcon Labs Hand Sanitizer Light Cleansing
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALCOHOL 600 mL/L
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 51801-779-08 Amcon Labs Hand Sanitizer Light Cleansing 0.237 L in 1 BOTTLE, PUMP SPRAY 0.237 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 51801-779 AMCON LABS HAND SANITIZER LIGHT CLEANSING (ALCOHOL) SPRAY [NOMAX, INC.] 2 Current NDC, 1 package rows 20231121_02187a0b-612b-e2e7-e063-6394a90abe70.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 1 of 1 · 1 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Sample Exclude flag Status 51801-779-08 51801077908 .237 L in 1 BOTTLE, PUMP (51801-779-08) 2023-08-04 No No Current