Home NDC 69842-265 CVS Medicated anti itch
Product NDC 69842-265
11-digit product format 698420265
Labeler code 69842
Product ID 69842-265_0c531457-76c7-6d06-e063-6394a90abb0d
Type HUMAN OTC DRUG
Nonproprietary name Pramoxine hydrochloride, menthol
Dosage form CREAM
Route TOPICAL
Labeler CVS
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2014-04-13
Substance PRAMOXINE HYDROCHLORIDE; MENTHOL
Active strength 1; 1 g/100g; g/100g
NDC exclude flag No
Listing certified through 2026-12-31
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 Medicated anti itch
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength PRAMOXINE HYDROCHLORIDE 1 g/100g MENTHOL 1 g/100g
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 L7T10EIP3A Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1116155 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 69842-265-01 CVS Medicated anti itch 1 in 1 CARTON CREAM 1 7 69842-265-01 CVS Medicated anti itch 28 g in 1 TUBE CREAM 28 7 69842-265-02 CVS Medicated anti itch 56 g in 1 TUBE CREAM 56 7 69842-265-02 CVS Medicated anti itch 1 in 1 CARTON CREAM 1 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69842-265 CVS MEDICATED ANTI ITCH (PRAMOXINE HYDROCHLORIDE, MENTHOL) CREAM [CVS] 7 Current NDC, Legacy NDC, 4 package rows 20231213_86972218-31fe-6942-e053-2991aa0a8850.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 108 of 152 · 3,029 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 69842-265-01 69842026501 1 TUBE in 1 CARTON (69842-265-01) / 28 g in 1 TUBE 1 tube 2014-04-13 0000-00-00 No No Current 69842-265-02 69842026502 1 TUBE in 1 CARTON (69842-265-02) / 56 g in 1 TUBE 1 tube 2014-04-13 No No Current