Home NDC 69842-400 CVS Itch Relief
Product NDC 69842-400
11-digit product format 698420400
Labeler code 69842
Product ID 69842-400_0cf95509-d4ee-83fb-e063-6394a90a4e08
Type HUMAN OTC DRUG
Nonproprietary name Pramoxine Hydrochloride and Zinc Acetate
Dosage form LOTION
Route TOPICAL
Labeler CVS Pharmacy
Application M016
Marketing category OTC MONOGRAPH DRUG
Marketing start 2008-01-01
Substance PRAMOXINE HYDROCHLORIDE; ZINC ACETATE
Active strength 10; 1 mg/mL; mg/mL
Pharmacologic classes Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [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 CVS Itch Relief
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength PRAMOXINE HYDROCHLORIDE 10 mg/mL ZINC ACETATE 1 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 88AYB867L5 Internal UNII lookup FM5526K07A Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1234546 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 69842-400-96 CVS Itch Relief 177 mL in 1 BOTTLE, PLASTIC LOTION 177 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69842-400 CVS ITCH RELIEF (PRAMOXINE HYDROCHLORIDE AND ZINC ACETATE) LOTION [CVS PHARMACY] 7 Current NDC, Legacy NDC, 1 package rows 20231221_c60cfbf2-6788-43dc-b23a-e3433b7f3265.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 52 of 68 · 1,350 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 69842-400-96 69842040096 177 mL in 1 BOTTLE, PLASTIC (69842-400-96) 177 ml 2008-01-01 0000-00-00 No No Current