Home NDC 21749-458 GOJO Antibacterial Ltn Sp
Product NDC 21749-458
11-digit product format 217490458
Labeler code 21749
Product ID 21749-458_4dcb9407-bc4d-b3f8-e063-6394a90ae035
Type HUMAN OTC DRUG
Nonproprietary name Chloroxylenol
Dosage form LIQUID
Route TOPICAL
Labeler GOJO Industries, Inc.
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-03-24
Substance CHLOROXYLENOL
Active strength .003 mg/mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base GOJO Antibacterial Ltn Sp
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CHLOROXYLENOL .003 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 0F32U78V2Q Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 21749-458-37 GOJO Antibacterial Ltn Sp 3780 mL in 1 PACKAGE LIQUID 3780 1
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.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 21749-458-37 21749045837 3780 mL in 1 PACKAGE (21749-458-37) 3780 ml 2026-03-24 No No Current