Home NDC 82442-088-07 UP and UP
Product NDC 82442-088
Requested package NDC 82442-088-07
11-digit product format 824420088
Labeler code 82442
Product ID 82442-088_51531f24-f43f-f7d9-e063-6294a90a0394
Type HUMAN OTC DRUG
Nonproprietary name Benzalkonium Chloride
Dosage form LIQUID
Route TOPICAL
Labeler TARGET CORPORATION INC.
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-10-22
Substance BENZALKONIUM CHLORIDE
Active strength 130 mg/100mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base UP and UP
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZALKONIUM CHLORIDE 130 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 1046593 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 82442-088-07 UP and UP 222 mL in 1 BOTTLE, PLASTIC LIQUID 222 5
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 82442-088-07 82442008807 222 mL in 1 BOTTLE, PLASTIC (82442-088-07) 222 ml 2025-10-22 No No Current