Home NDC 69842-952 CVS Itch Relief
Product NDC 69842-952
11-digit product format 698420952
Labeler code 69842
Product ID 69842-952_4369c991-f8ec-14db-e063-6394a90ad1e1
Type HUMAN OTC DRUG
Nonproprietary name Diphenhydramine HCl, Zinc Acetate
Dosage form SPRAY
Route TOPICAL
Labeler CVS
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2014-04-14
Substance ZINC ACETATE; DIPHENHYDRAMINE HYDROCHLORIDE
Active strength .1; 2 g/100mL; g/100mL
Pharmacologic classes Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
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 Itch Relief
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC ACETATE .1 g/100mL DIPHENHYDRAMINE HYDROCHLORIDE 2 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination FM5526K07A Internal UNII lookup TC2D6JAD40 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1053138 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 69842-952-02 CVS Itch Relief 59 mL in 1 BOTTLE, SPRAY SPRAY 59 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69842-952 CVS ITCH RELIEF (DIPHENHYDRAMINE HCL, ZINC ACETATE) SPRAY [CVS] 1 Current NDC, Legacy NDC, 1 package rows 20190424_8723e097-296f-784a-e053-2991aa0a552e.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 18 of 153 · 3,057 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 69842-952-02 69842095202 59 mL in 1 BOTTLE, SPRAY (69842-952-02) 59 ml 2014-04-14 0000-00-00 No No Current