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
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
F5UM2KM3W7BENZALKONIUM CHLORIDE8001-54-5BENZALKONIUM CHLORIDE
V13007Z41ALIDOCAINE HYDROCHLORIDE6108-05-0LIDOCAINE HYDROCHLORIDE

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
82442-018-2182442001821150 mL in 1 BOTTLE (82442-018-21) 150 ml2025-01-14NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Up and Up Max Pain Relieving Cleansing SprayTARGET CORPORATION2025-01-21HUMAN OTC DRUG LABEL1