Home NDC 37808-932 Allergy Relief
Product NDC 37808-932
11-digit product format 378080932
Labeler code 37808
Product ID 37808-932_791c6ee6-ee0a-402f-8d64-ee77af8d01f5
Type HUMAN OTC DRUG
Nonproprietary name Diphenhydramine HCl
Dosage form TABLET, FILM COATED
Route ORAL
Labeler H E B
Application M012
Marketing category OTC MONOGRAPH DRUG
Marketing start 1990-03-02
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 Relief
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 37808-932-08 Allergy Relief 12 in 1 BLISTER PACK TABLET, FILM COATED 12 13 37808-932-08 Allergy Relief 2 in 1 CARTON TABLET, FILM COATED 2 13 37808-932-78 Allergy Relief 600 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 600 13
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 37808-932 ALLERGY RELIEF (DIPHENHYDRAMINE HCL) TABLET, FILM COATED [H E B] 12 Current NDC, Legacy NDC, 3 package rows 20250105_c9e977b6-fba6-49ea-9d80-b43b0842bbe1.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 37808-932-08 37808093208 2 BLISTER PACK in 1 CARTON (37808-932-08) / 12 TABLET, FILM COATED in 1 BLISTER PACK 2 blister pack 1990-03-02 0000-00-00 No No Current 37808-932-78 37808093278 600 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (37808-932-78) 1990-03-02 0000-00-00 No No Current