Home NDC 82442-018 Up and Up Max Pain Relieving Cleansing
Product NDC 82442-018
11-digit product format 824420018
Labeler code 82442
Product ID 82442-018_2c3e8149-f59a-4b05-e063-6394a90ad10b
Type HUMAN OTC DRUG
Nonproprietary name Benzalkonium Chloride and Lidocaine Hydrochloride
Dosage form LIQUID
Route TOPICAL
Labeler TARGET CORPORATION
Application M003
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-01-14
Substance BENZALKONIUM CHLORIDE; LIDOCAINE HYDROCHLORIDE
Active strength .13; 4 g/100mL; g/100mL
Pharmacologic classes Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE]
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 Up and Up Max Pain Relieving Cleansing
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZALKONIUM CHLORIDE .13 g/100mL LIDOCAINE HYDROCHLORIDE 4 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination F5UM2KM3W7 Internal UNII lookup V13007Z41A Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2047877 Internal RxNorm 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 82442-018-21 Up and Up Max Pain Relieving Cleansing 150 mL in 1 BOTTLE LIQUID 150 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 82442-018 UP AND UP MAX PAIN RELIEVING CLEANSING (BENZALKONIUM CHLORIDE AND LIDOCAINE HYDROCHLORIDE) LIQUID [TARGET CORPORATION] 1 Current NDC, 1 package rows 20250123_2c3e72eb-5d98-1f3f-e063-6394a90ab00c.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 9 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 82442-018-21 82442001821 150 mL in 1 BOTTLE (82442-018-21) 150 ml 2025-01-14 No No Current