Home NDC 59448-003 Instant Hand Antiseptic
Product NDC 59448-003
11-digit product format 594480003
Labeler code 59448
Product ID 59448-003_c5011eba-9aad-4a0c-a4e1-40b10df0402c
Type HUMAN OTC DRUG
Nonproprietary name Benzalkonium Chloride
Dosage form GEL
Route TOPICAL
Labeler ASP Global
Application M003
Marketing category OTC MONOGRAPH DRUG
Marketing start 2018-11-27
Substance BENZALKONIUM CHLORIDE
Active strength .095 mg/100mL
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 Instant Hand Antiseptic
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZALKONIUM CHLORIDE .095 mg/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 2048259 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 59448-003-01 Univ of Vermont Medical Center Amenity 53 mL in 1 BOTTLE, PLASTIC GEL 53 mL 0.095 mg in 100mL 5 59448-003-01 Instant Hand Antiseptic 53 mL in 1 BOTTLE, PLASTIC GEL 53 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 59448-003 INSTANT HAND ANTISEPTIC (BENZALKONIUM CHLORIDE) GEL [ASP GLOBAL] 5 Current NDC, Legacy NDC, 1 package rows 20241208_47276148-08e5-400e-94ac-d2d9db423b51.zip 59448-003 UNIV OF VERMONT MEDICAL CENTER AMENITY (BENZALKONIUM CHLORIDE AND SODIUM MONOFLUOROPHOSPHATE) KIT [ASP GLOBAL, LLC] 5 Current NDC, Legacy NDC 20241222_7841cfa9-e94e-4c3d-b5fb-676924017845.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 86 of 115 · 2,286 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 59448-003-01 59448000301 53 mL in 1 BOTTLE, PLASTIC (59448-003-01) 53 ml 2018-11-27 0000-00-00 No No Current