Home NDC 71679-106 Allergy Relief
Product NDC 71679-106
11-digit product format 716790106
Labeler code 71679
Product ID 71679-106_55feb1c4-8bfd-1cd5-e063-6394a90af306
Type HUMAN OTC DRUG
Nonproprietary name Diphenhydramine Hydrochloride
Dosage form TABLET
Route ORAL
Labeler Health Pharma USA LLC
Application M012
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-06-24
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 71679-106-01 Allergy Relief 100 in 1 BOTTLE TABLET 100 31 71679-106-03 Allergy Relief 300 in 1 BOTTLE TABLET 300 31 71679-106-06 Allergy Relief 600 in 1 BOTTLE TABLET 600 31 71679-106-10 Allergy Relief 1000 in 1 BOTTLE TABLET 1000 31
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71679-106 ALLERGY RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET [HEALTH PHARMA USA LLC] 29 Current NDC, Legacy NDC, 4 package rows 20231031_d38f47ea-7fda-170b-e053-2995a90adc82.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 73 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 Marketing end Sample Exclude flag Status 71679-106-01 71679010601 100 TABLET in 1 BOTTLE (71679-106-01) 100 tablet 2025-06-24 No No Current 71679-106-03 71679010603 300 TABLET in 1 BOTTLE (71679-106-03) 300 tablet 2025-06-24 No No Current 71679-106-06 71679010606 600 TABLET in 1 BOTTLE (71679-106-06) 600 tablet 2025-06-24 0000-00-00 No No Current 71679-106-10 71679010610 1000 TABLET in 1 BOTTLE (71679-106-10) 1000 tablet 2025-06-24 0000-00-00 No No Current