Home NDC 79481-0598 Extra Strength Itch Relief
Product NDC 79481-0598
11-digit product format 794810598
Labeler code 79481
Product ID 79481-0598_426612e5-5b40-749b-e063-6294a90a3968
Type HUMAN OTC DRUG
Nonproprietary name Diphenhydramine HCl and Zinc Acetate
Dosage form SPRAY
Route TOPICAL
Labeler Meijer Distribution Inc
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-08-15
Substance DIPHENHYDRAMINE HYDROCHLORIDE; ZINC ACETATE
Active strength 20; 1 mg/g; mg/g
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 Extra Strength Itch Relief
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength DIPHENHYDRAMINE HYDROCHLORIDE 20 mg/g ZINC ACETATE 1 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination TC2D6JAD40 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 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 79481-0598-1 Extra Strength Itch Relief 76 g in 1 CAN SPRAY 76 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 79481-0598 EXTRA STRENGTH ITCH RELIEF (DIPHENHYDRAMINE HCL AND ZINC ACETATE) SPRAY [MEIJER DISTRIBUTION INC] 3 Current NDC, 1 package rows 20241016_02f9e270-6047-83b6-e063-6394a90afc27.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 Sample Exclude flag Status 79481-0598-1 79481059801 76 g in 1 CAN (79481-0598-1) 76 g 2023-08-15 No No Current