pain relief non drowsy daytime

Generic: acetaminophen, phenylephrine hcl

Labeler: better living brands, llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name pain relief non drowsy daytime
Generic Name acetaminophen, phenylephrine hcl
Labeler better living brands, llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

acetaminophen 325 mg/1, phenylephrine hydrochloride 5 mg/1

Manufacturer
Better Living Brands, LLC

Identifiers & Regulatory

Product NDC 21130-466
Product ID 21130-466_bbea4153-0f97-4d3e-93c7-0e3c3d0942a6
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Marketing Start 2005-07-26
Marketing End 2026-07-23

Pharmacologic Class

Classes
adrenergic alpha1-agonists [moa] alpha-1 adrenergic agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 21130466
Hyphenated Format 21130-466

Supplemental Identifiers

RxCUI
1046378
UPC
0321130787921
UNII
362O9ITL9D 04JA59TNSJ

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 pain relief non drowsy daytime (source: ndc)
Generic Name acetaminophen, phenylephrine hcl (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 325 mg/1
  • 5 mg/1
source: ndc
Packaging
  • 2 BLISTER PACK in 1 CARTON (21130-466-08) / 12 TABLET, FILM COATED in 1 BLISTER PACK
source: ndc

Packages (1)

Ingredients (2)

acetaminophen (325 mg/1) phenylephrine hydrochloride (5 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "bbea4153-0f97-4d3e-93c7-0e3c3d0942a6", "openfda": {"upc": ["0321130787921"], "unii": ["362O9ITL9D", "04JA59TNSJ"], "rxcui": ["1046378"], "spl_set_id": ["fb4d0f19-96bb-4611-9f23-436cf47f6f0f"], "manufacturer_name": ["Better Living Brands, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (21130-466-08)  / 12 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "21130-466-08", "marketing_end_date": "20260723", "marketing_start_date": "20050726"}], "brand_name": "Pain Relief Non Drowsy Daytime", "product_id": "21130-466_bbea4153-0f97-4d3e-93c7-0e3c3d0942a6", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "21130-466", "generic_name": "Acetaminophen, Phenylephrine HCl", "labeler_name": "Better Living Brands, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Relief", "brand_name_suffix": "Non Drowsy Daytime", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20260723", "marketing_start_date": "20050726"}