somnapure clinical strength

Generic: diphenhydramine hydrochloride

Labeler: force factor brands llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name somnapure clinical strength
Generic Name diphenhydramine hydrochloride
Labeler force factor brands llc
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

diphenhydramine hydrochloride 50 mg/1

Manufacturer
Force Factor Brands LLC

Identifiers & Regulatory

Product NDC 69721-005
Product ID 69721-005_35de71a0-7e1c-45fb-97d1-ddf485df6e3c
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M010
Listing Expiration 2026-12-31
Marketing Start 2018-03-20

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 69721005
Hyphenated Format 69721-005

Supplemental Identifiers

RxCUI
1085945 1609070
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 somnapure clinical strength (source: ndc)
Generic Name diphenhydramine hydrochloride (source: ndc)
Application Number M010 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (69721-005-30) / 30 TABLET, COATED in 1 BOTTLE
source: ndc

Packages (1)

69721-005-30 1 BOTTLE in 1 CARTON (69721-005-30) / 30 TABLET, COATED in 1 BOTTLE

Ingredients (1)

diphenhydramine hydrochloride (50 mg/1)

Linked Drug Pages (1)

Somnapure Clinical Strength ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "35de71a0-7e1c-45fb-97d1-ddf485df6e3c", "openfda": {"unii": ["TC2D6JAD40"], "rxcui": ["1085945", "1609070"], "spl_set_id": ["063517c0-bcb1-46dd-85f1-bbb2f24274ef"], "manufacturer_name": ["Force Factor Brands LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (69721-005-30)  / 30 TABLET, COATED in 1 BOTTLE", "package_ndc": "69721-005-30", "marketing_start_date": "20180320"}], "brand_name": "Somnapure Clinical Strength", "product_id": "69721-005_35de71a0-7e1c-45fb-97d1-ddf485df6e3c", "dosage_form": "TABLET, COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "69721-005", "generic_name": "Diphenhydramine Hydrochloride", "labeler_name": "Force Factor Brands LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Somnapure", "brand_name_suffix": "Clinical Strength", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "M010", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20180320", "listing_expiration_date": "20261231"}