Home NDC 46122-829 Allergy Relief
Product NDC 46122-829
11-digit product format 461220829
Labeler code 46122
Product ID 46122-829_5d1a39bf-a510-eb7f-e063-6394a90a7e57
Type HUMAN OTC DRUG
Nonproprietary name Diphenhydramine HCl
Dosage form TABLET
Route ORAL
Labeler AMERISOURCE BERGEN
Application M012
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-05-04
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
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength DIPHENHYDRAMINE HYDROCHLORIDE 50 mg/1
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 46122-829-51 Allergy Relief 12 in 1 BLISTER PACK TABLET 12 1 46122-829-51 Allergy Relief 2 in 1 CARTON TABLET 2 1
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 Sample Exclude flag Status 46122-829-51 46122082951 2 BLISTER PACK in 1 CARTON (46122-829-51) / 12 TABLET in 1 BLISTER PACK 2 blister pack 2026-05-04 No No Current