allergy relief
Generic: diphenhydramine hydrochloride
Labeler: twin med llcDrug Facts
Product Profile
Brand Name
allergy relief
Generic Name
diphenhydramine hydrochloride
Labeler
twin med llc
Dosage Form
TABLET
Routes
Active Ingredients
diphenhydramine hydrochloride 25 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
55681-323
Product ID
55681-323_3906f36f-58a1-4299-e063-6394a90a30df
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M012
Listing Expiration
2026-12-31
Marketing Start
2024-11-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
55681323
Hyphenated Format
55681-323
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 25 mg/1
Packaging
- 300 TABLET in 1 BOTTLE (55681-323-03)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3906f36f-58a1-4299-e063-6394a90a30df", "openfda": {"unii": ["TC2D6JAD40"], "rxcui": ["1049630"], "spl_set_id": ["7b000478-649d-4511-b3e0-eea6995b9784"], "manufacturer_name": ["TWIN MED LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "300 TABLET in 1 BOTTLE (55681-323-03)", "package_ndc": "55681-323-03", "marketing_start_date": "20241101"}], "brand_name": "Allergy Relief", "product_id": "55681-323_3906f36f-58a1-4299-e063-6394a90a30df", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "55681-323", "generic_name": "Diphenhydramine Hydrochloride", "labeler_name": "TWIN MED 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": "20241101", "listing_expiration_date": "20261231"}