Home NDC 71884-016-01 Germfree24 Hand Sanitizer
Product NDC 71884-016
Requested package NDC 71884-016-01
11-digit product format 718840016
Labeler code 71884
Product ID 71884-016_41c21635-d8b4-4856-b1cf-2f2b93b1b78b
Type HUMAN OTC DRUG
Nonproprietary name Benzalkonium Chloride
Dosage form SPRAY
Route TOPICAL
Labeler Enviro Specialty Chemicals Inc
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-12-17
Substance BENZALKONIUM CHLORIDE
Active strength .13 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 Germfree24 Hand Sanitizer
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZALKONIUM CHLORIDE .13 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 1039012 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 71884-016-01 Germfree24 Hand Sanitizer 10 mL in 1 BOTTLE, SPRAY SPRAY 10 2 71884-016-02 Germfree24 Hand Sanitizer 57 mL in 1 BOTTLE, SPRAY SPRAY 57 2 71884-016-03 Germfree24 Hand Sanitizer 200 mL in 1 BOTTLE, SPRAY SPRAY 200 2 71884-016-04 Germfree24 Hand Sanitizer 250 mL in 1 BOTTLE, SPRAY SPRAY 250 2 71884-016-05 Germfree24 Hand Sanitizer 473 mL in 1 BOTTLE, SPRAY SPRAY 473 2 71884-016-06 Germfree24 Hand Sanitizer 3785 mL in 1 BOTTLE, SPRAY SPRAY 3785 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71884-016 GERMFREE24 HAND SANITIZER (BENZALKONIUM CHLORIDE) SPRAY [ENVIRO SPECIALTY CHEMICALS INC] 2 Current NDC, Legacy NDC, 6 package rows 20250106_fb43545b-6ddc-49fb-86dd-17cd1a925a78.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 Units Marketing start Marketing end Sample Exclude flag Status 71884-016-01 71884001601 10 mL in 1 BOTTLE, SPRAY (71884-016-01) 10 ml 2020-12-17 0000-00-00 No No Current