allergy relief

Generic: diphenhydramine hydrochloride

Labeler: topco associates llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name allergy relief
Generic Name diphenhydramine hydrochloride
Labeler topco associates llc
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

diphenhydramine hydrochloride 25 mg/1

Manufacturer
TopCo Associates LLC

Identifiers & Regulatory

Product NDC 36800-909
Product ID 36800-909_2850dd0b-fd81-c211-e063-6394a90a77ca
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2011-08-30

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 36800909
Hyphenated Format 36800-909

Supplemental Identifiers

RxCUI
1049630
UPC
0036800332430
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
  • 2 BLISTER PACK in 1 CARTON (36800-909-01) / 12 TABLET, COATED in 1 BLISTER PACK
  • 4 BLISTER PACK in 1 CARTON (36800-909-02) / 12 TABLET, COATED in 1 BLISTER PACK
source: ndc

Packages (2)

36800-909-01 2 BLISTER PACK in 1 CARTON (36800-909-01) / 12 TABLET, COATED in 1 BLISTER PACK 36800-909-02 4 BLISTER PACK in 1 CARTON (36800-909-02) / 12 TABLET, COATED in 1 BLISTER PACK

Ingredients (1)

diphenhydramine hydrochloride (25 mg/1)

Linked Drug Pages (1)

Allergy Relief ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2850dd0b-fd81-c211-e063-6394a90a77ca", "openfda": {"upc": ["0036800332430"], "unii": ["TC2D6JAD40"], "rxcui": ["1049630"], "spl_set_id": ["53b15e75-9efd-4b4b-834b-6e9f12c60108"], "manufacturer_name": ["TopCo Associates LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (36800-909-01)  / 12 TABLET, COATED in 1 BLISTER PACK", "package_ndc": "36800-909-01", "marketing_start_date": "20110830"}, {"sample": false, "description": "4 BLISTER PACK in 1 CARTON (36800-909-02)  / 12 TABLET, COATED in 1 BLISTER PACK", "package_ndc": "36800-909-02", "marketing_start_date": "20110830"}], "brand_name": "Allergy Relief", "product_id": "36800-909_2850dd0b-fd81-c211-e063-6394a90a77ca", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "36800-909", "generic_name": "DIPHENHYDRAMINE HYDROCHLORIDE", "labeler_name": "TopCo Associates LLC", "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": "20110830", "listing_expiration_date": "20261231"}