Home NDC 80659-301 Purifi Hand Sanitizer
Product NDC 80659-301
11-digit product format 806590301
Labeler code 80659
Product ID 80659-301_103dc041-e75d-b464-e063-6394a90ab4d8
Type HUMAN OTC DRUG
Nonproprietary name Benzalkonium chloride
Dosage form SOLUTION
Route TOPICAL
Labeler Purifi LLC
Application M007
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-12-10
Substance BENZALKONIUM CHLORIDE
Active strength .13 g/100mL
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 Purifi Hand Sanitizer
Listing expiration 2026-12-31 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 1049254 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 80659-301-01 Purifi Hand Sanitizer 250 mL in 1 BOTTLE, PLASTIC SOLUTION 250 4 80659-301-02 Purifi Hand Sanitizer 60 mL in 1 BOTTLE, PLASTIC SOLUTION 60 4 80659-301-03 Purifi Hand Sanitizer 3800 mL in 1 BOTTLE, PLASTIC SOLUTION 3800 4 80659-301-04 Purifi Hand Sanitizer 50 mL in 1 BOTTLE, PLASTIC SOLUTION 50 4 80659-301-05 Purifi Hand Sanitizer 296 mL in 1 BOTTLE, PLASTIC SOLUTION 296 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 80659-301 PURIFI HAND SANITIZER (BENZALKONIUM CHLORIDE) SOLUTION [PURIFI LLC] 4 Current NDC, Legacy NDC, 5 package rows 20240201_9267069d-4cf5-4e48-a446-7dbebea16bf5.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 14 of 42 · 833 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 80659-301-01 80659030101 250 mL in 1 BOTTLE, PLASTIC (80659-301-01) 250 ml 2020-12-10 0000-00-00 No No Current 80659-301-02 80659030102 60 mL in 1 BOTTLE, PLASTIC (80659-301-02) 60 ml 2020-12-10 0000-00-00 No No Current 80659-301-03 80659030103 3800 mL in 1 BOTTLE, PLASTIC (80659-301-03) 3800 ml 2020-12-10 0000-00-00 No No Current 80659-301-04 80659030104 50 mL in 1 BOTTLE, PLASTIC (80659-301-04) 50 ml 2020-12-10 0000-00-00 No No Current 80659-301-05 80659030105 296 mL in 1 BOTTLE, PLASTIC (80659-301-05) 296 ml 2020-12-10 0000-00-00 No No Current