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
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
F5UM2KM3W7BENZALKONIUM CHLORIDE8001-54-5BENZALKONIUM CHLORIDE

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
80659-301-0180659030101250 mL in 1 BOTTLE, PLASTIC (80659-301-01) 250 ml2020-12-10NoNoHistorical
80659-301-028065903010260 mL in 1 BOTTLE, PLASTIC (80659-301-02) 60 ml2020-12-10NoNoHistorical
80659-301-03806590301033800 mL in 1 BOTTLE, PLASTIC (80659-301-03) 3800 ml2020-12-10NoNoHistorical
80659-301-048065903010450 mL in 1 BOTTLE, PLASTIC (80659-301-04) 50 ml2020-12-10NoNoHistorical
80659-301-0580659030105296 mL in 1 BOTTLE, PLASTIC (80659-301-05) 296 ml2020-12-10NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Purifi Moisturizing Hand Sanitizer INSTANTLY KILLS 99.99% OF TESTED GERMSPurifi LLC2024-01-31HUMAN OTC DRUG LABEL4