allergy relief

Generic: diphenhydramine hydrochloride

Labeler: chain drug marketing association, inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name allergy relief
Generic Name diphenhydramine hydrochloride
Labeler chain drug marketing association, inc.
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

diphenhydramine hydrochloride 25 mg/1

Manufacturer
CHAIN DRUG MARKETING ASSOCIATION, INC.

Identifiers & Regulatory

Product NDC 83324-088
Product ID 83324-088_1f7f0940-6e4b-41d1-e063-6294a90a4e5b
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2024-08-12

Pharmacologic Class

Classes
histamine h1 receptor antagonists [moa] histamine-1 receptor antagonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 83324088
Hyphenated Format 83324-088

Supplemental Identifiers

RxCUI
1049630
UPC
0635515945777
UNII
TC2D6JAD40

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name allergy relief (source: ndc)
Generic Name diphenhydramine hydrochloride (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 1 BOTTLE, PLASTIC in 1 CARTON (83324-088-01) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC
  • 1 BOTTLE, PLASTIC in 1 CARTON (83324-088-03) / 300 TABLET, COATED in 1 BOTTLE, PLASTIC
  • 2 BLISTER PACK in 1 CARTON (83324-088-24) / 12 TABLET, COATED in 1 BLISTER PACK
source: ndc

Packages (3)

Ingredients (1)

diphenhydramine hydrochloride (25 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1f7f0940-6e4b-41d1-e063-6294a90a4e5b", "openfda": {"upc": ["0635515945777"], "unii": ["TC2D6JAD40"], "rxcui": ["1049630"], "spl_set_id": ["445e49a2-6ed0-434c-aaea-3ce14bc7df59"], "manufacturer_name": ["CHAIN DRUG MARKETING ASSOCIATION, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (83324-088-01)  / 100 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "83324-088-01", "marketing_start_date": "20240812"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (83324-088-03)  / 300 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "83324-088-03", "marketing_start_date": "20240812"}, {"sample": false, "description": "2 BLISTER PACK in 1 CARTON (83324-088-24)  / 12 TABLET, COATED in 1 BLISTER PACK", "package_ndc": "83324-088-24", "marketing_start_date": "20240812"}], "brand_name": "Allergy Relief", "product_id": "83324-088_1f7f0940-6e4b-41d1-e063-6294a90a4e5b", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "83324-088", "generic_name": "DIPHENHYDRAMINE HYDROCHLORIDE", "labeler_name": "CHAIN DRUG MARKETING ASSOCIATION, INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Allergy Relief", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240812", "listing_expiration_date": "20261231"}