Home NDC 50580-322 Benadryl Allergy Extra Strength Liqui-Gels
Product NDC 50580-322
11-digit product format 505800322
Labeler code 50580
Product ID 50580-322_451a21a1-4357-d575-e063-6394a90a900a
Type HUMAN OTC DRUG
Nonproprietary name Diphenhydramine Hydrochloride
Dosage form CAPSULE, LIQUID FILLED
Route ORAL
Labeler Kenvue Brands LLC
Application M012
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-05-15
Marketing end 2027-04-30
Substance DIPHENHYDRAMINE HCL
Active strength 50 mg/1
Pharmacologic classes Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
NDC exclude flag No
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 Benadryl Allergy Extra Strength Liqui-Gels Active Ingredients# Ingredient, Strength table Ingredient Strength DIPHENHYDRAMINE HCL 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 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1020477 Internal RxNorm lookup 1050076 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 50580-322-20 Benadryl Allergy Extra Strength Liqui-Gels 2 in 1 CARTON CAPSULE, LIQUID FILLED 2 3 50580-322-20 Benadryl Allergy Extra Strength Liqui-Gels 10 in 1 BLISTER PACK CAPSULE, LIQUID FILLED 10 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 50580-322 BENADRYL ALLERGY EXTRA STRENGTH LIQUI-GELS (DIPHENHYDRAMINE HYDROCHLORIDE) CAPSULE, LIQUID FILLED [KENVUE BRANDS LLC] 2 Current NDC, 2 package rows 20250523_30aca3ab-b091-3939-e063-6294a90a9819.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 74 of 180 · 3,583 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 50580-322-20 50580032220 2 BLISTER PACK in 1 CARTON (50580-322-20) / 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK 2 blister pack 2025-05-15 2027-04-30 No No Historical