United States · FDA National Drug Code directory
Purifi Hand Sanitizer
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 80659-301_103dc041-e75d-b464-e063-6394a90ab4d8
- Product NDC
- 80659-301
- Form
- SOLUTION
- Composition / generic term
- Benzalkonium chloride
- Labeler
- Purifi LLC
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20201210
- Source listing expiry
- 20261231
Source-listed ingredients
- BENZALKONIUM CHLORIDE — .13 g/100mL
These values do not establish equivalence or a dose recommendation.
Packages
- 250 mL in 1 BOTTLE, PLASTIC (80659-301-01) · 80659-301-01
- 60 mL in 1 BOTTLE, PLASTIC (80659-301-02) · 80659-301-02
- 3800 mL in 1 BOTTLE, PLASTIC (80659-301-03) · 80659-301-03
- 50 mL in 1 BOTTLE, PLASTIC (80659-301-04) · 80659-301-04
- 296 mL in 1 BOTTLE, PLASTIC (80659-301-05) · 80659-301-05
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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