Home NDC 71884-203 DOCTOR INKS TOPICAL ANTISEPTIC
Product NDC 71884-203
11-digit product format 718840203
Labeler code 71884
Product ID 71884-203_1984543f-4ded-41ba-acf8-5e3813680672
Type HUMAN OTC DRUG
Nonproprietary name Benzalkonium Chloride
Dosage form GEL
Route TOPICAL
Labeler Enviro Specialty Chemicals Inc
Application M003
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 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 DOCTOR INKS TOPICAL ANTISEPTIC
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 1098199 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 71884-203-01 DOCTOR INKS TOPICAL ANTISEPTIC 30 mL in 1 TUBE GEL 30 2 71884-203-02 DOCTOR INKS TOPICAL ANTISEPTIC 59 mL in 1 TUBE GEL 59 2 71884-203-03 DOCTOR INKS TOPICAL ANTISEPTIC 118 mL in 1 TUBE GEL 118 2 71884-203-04 DOCTOR INKS TOPICAL ANTISEPTIC 237 mL in 1 TUBE GEL 237 2 71884-203-05 DOCTOR INKS TOPICAL ANTISEPTIC 3785 mL in 1 JUG GEL 3785 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71884-203 DOCTOR INKS TOPICAL ANTISEPTIC (BENZALKONIUM CHLORIDE) GEL [ENVIRO SPECIALTY CHEMICALS INC] 2 Current NDC, 5 package rows 20250106_d503a2db-e326-4a31-bc6a-5034ad74bf0b.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 101 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 Sample Exclude flag Status 71884-203-01 71884020301 30 mL in 1 TUBE (71884-203-01) 30 ml 2022-09-01 No No Current 71884-203-02 71884020302 59 mL in 1 TUBE (71884-203-02) 59 ml 2022-09-01 No No Current 71884-203-03 71884020303 118 mL in 1 TUBE (71884-203-03) 118 ml 2022-09-01 No No Current 71884-203-04 71884020304 237 mL in 1 TUBE (71884-203-04) 237 ml 2022-09-01 No No Current 71884-203-05 71884020305 3785 mL in 1 JUG (71884-203-05) 3785 ml 2022-09-01 No No Current