Home NDC 72202-282 Zogics Foam Hand Sanitizer
Product NDC 72202-282
11-digit product format 722020282
Labeler code 72202
Product ID 72202-282_36e8b7a6-4e3c-378e-e063-6394a90a2652
Type HUMAN OTC DRUG
Nonproprietary name Benzalakonium
Dosage form LIQUID
Route TOPICAL
Labeler Zogics, LLC
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2017-04-24
Substance BENZALKONIUM CHLORIDE
Active strength .12 g/100mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Zogics Foam Hand Sanitizer
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZALKONIUM CHLORIDE .12 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination F5UM2KM3W7 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1046310 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 72202-282-00 Zogics Foam Hand Sanitizer 3785 mL in 1 BOTTLE, PLASTIC LIQUID 3785 1
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 Units Marketing start Sample Exclude flag Status 72202-282-00 72202028200 3785 mL in 1 BOTTLE, PLASTIC (72202-282-00) 3785 ml 2017-04-24 No No Current