Home NDC 73581-020 Allergy Relief Diphenhydramine HCL 50 MG
Product NDC 73581-020
11-digit product format 735810020
Labeler code 73581
Product ID 73581-020_485e261c-d3c1-2b7e-e063-6394a90abecd
Type HUMAN OTC DRUG
Nonproprietary name Diphenhydramine HCL
Dosage form CAPSULE
Route ORAL
Labeler YYBA Corporation
Application M012
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-08-01
Substance DIPHENHYDRAMINE HYDROCHLORIDE
Active strength 50 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 Relief Diphenhydramine HCL 50 MG
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength DIPHENHYDRAMINE HYDROCHLORIDE 50 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 1020477 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 73581-020-05 Allergy Relief Diphenhydramine HCL 50 MG 50 in 1 BOTTLE, PLASTIC CAPSULE 50 3 73581-020-10 Allergy Relief Diphenhydramine HCL 50 MG 1000 in 1 BOTTLE, PLASTIC CAPSULE 1000 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 73581-020 ALLERGY RELIEF DIPHENHYDRAMINE HCL 50 MG (DIPHENHYDRAMINE HCL) CAPSULE [YYBA CORPORATION] 2 Current NDC, 2 package rows 20241212_4b012549-3958-43c1-9de7-897c5d8b20d3.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 151 of 177 · 3,534 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 73581-020-05 73581002005 50 CAPSULE in 1 BOTTLE, PLASTIC (73581-020-05) 50 capsule 2023-08-01 No No Current 73581-020-10 73581002010 1000 CAPSULE in 1 BOTTLE, PLASTIC (73581-020-10) 1000 capsule 2023-08-01 No No Current