Home NDC 78164-101 Hand Sanitizer plus Holder
Product NDC 78164-101
11-digit product format 781640101
Labeler code 78164
Product ID 78164-101_3f042aa7-7546-a06c-e063-6394a90aed31
Type HUMAN OTC DRUG
Nonproprietary name Benzalkonium Chloride
Dosage form LIQUID
Route TOPICAL
Labeler Gertex Hosiery
Application M003
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-09-01
Substance BENZALKONIUM CHLORIDE
Active strength .1 g/mL
NDC exclude flag No
Listing certified through 2026-12-31
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 Hand Sanitizer plus Holder
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZALKONIUM CHLORIDE .1 g/mL
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 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 78164-101-35 Hand Sanitizer plus Holder 35 mL in 1 BOTTLE LIQUID 35 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 92 of 115 · 2,286 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 78164-101-35 78164010135 35 mL in 1 BOTTLE (78164-101-35) 35 ml 2025-09-01 No No Current