Home NDC 71884-201-06 DOCTOR INKS HAND SANITIZER
Product NDC 71884-201
Requested package NDC 71884-201-06
11-digit product format 718840201
Labeler code 71884
Product ID 71884-201_a2f03511-5bc5-4bca-b598-ea8c81926298
Type HUMAN OTC DRUG
Nonproprietary name Benzalkonium Chloride
Dosage form LIQUID
Route TOPICAL
Labeler Enviro Specialty Chemicals Inc
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2022-09-01
Substance BENZALKONIUM CHLORIDE
Active strength 1.3 mg/mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base DOCTOR INKS HAND SANITIZER
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZALKONIUM CHLORIDE 1.3 mg/mL
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 1020365 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 71884-201-01 DOCTOR INKS HAND SANITIZER 58 mL in 1 BOTTLE, PUMP LIQUID 58 2 71884-201-02 DOCTOR INKS HAND SANITIZER 118 mL in 1 BOTTLE, PUMP LIQUID 118 2 71884-201-03 DOCTOR INKS HAND SANITIZER 244 mL in 1 BOTTLE, PUMP LIQUID 244 2 71884-201-04 DOCTOR INKS HAND SANITIZER 473 mL in 1 BOTTLE, PUMP LIQUID 473 2 71884-201-05 DOCTOR INKS HAND SANITIZER 1182 mL in 1 BAG LIQUID 1182 2 71884-201-06 DOCTOR INKS HAND SANITIZER 3785 mL in 1 JUG LIQUID 3785 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71884-201 DOCTOR INKS HAND SANITIZER (BENZALKONIUM CHLORIDE) LIQUID [ENVIRO SPECIALTY CHEMICALS INC] 2 Current NDC, 6 package rows 20250106_e174f231-73df-464b-bd92-23222659df24.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 Sample Exclude flag Status 71884-201-06 71884020106 3785 mL in 1 JUG (71884-201-06) 3785 ml 2022-09-01 No No Current