Home NDC 56062-923 Allergy
Product NDC 56062-923
11-digit product format 560620923
Labeler code 56062
Product ID 56062-923_f16600d1-e885-4659-b316-fd4cdde98455
Type HUMAN OTC DRUG
Nonproprietary name Diphenhydramine HCl
Dosage form TABLET, FILM COATED
Route ORAL
Labeler Publix Super Markets Inc
Application M012
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-04-28
Substance DIPHENHYDRAMINE HYDROCHLORIDE
Active strength 25 mg/1
Pharmacologic classes Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
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 Allergy
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength DIPHENHYDRAMINE HYDROCHLORIDE 25 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 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 1049630 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 56062-923-08 Allergy 12 in 1 BLISTER PACK TABLET, FILM COATED 12 3 56062-923-08 Allergy 2 in 1 CARTON TABLET, FILM COATED 2 3 56062-923-12 Allergy 1 in 1 CARTON TABLET, FILM COATED 1 3 56062-923-12 Allergy 100 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 100 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 56062-923 ALLERGY (DIPHENHYDRAMINE HCL) TABLET, FILM COATED [PUBLIX SUPER MARKETS INC] 2 Current NDC, 4 package rows 20250429_f2263e38-f686-45ed-bf85-b47f5e1aa982.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 97 of 178 · 3,551 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 56062-923-08 56062092308 2 BLISTER PACK in 1 CARTON (56062-923-08) / 12 TABLET, FILM COATED in 1 BLISTER PACK 2 blister pack 2025-04-28 No No Current 56062-923-12 56062092312 1 BOTTLE, PLASTIC in 1 CARTON (56062-923-12) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC 2025-04-28 No No Current