severe sinus daytime, non-drowsy

Generic: acetaminophen, guaifenesin, phenylephrine hcl

Labeler: walgreen company
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name severe sinus daytime, non-drowsy
Generic Name acetaminophen, guaifenesin, phenylephrine hcl
Labeler walgreen company
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

acetaminophen 325 mg/1, guaifenesin 200 mg/1, phenylephrine hydrochloride 5 mg/1

Manufacturer
Walgreen Company

Identifiers & Regulatory

Product NDC 0363-5027
Product ID 0363-5027_d8d12628-e9e4-4ab8-be43-1ef1538eeca3
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2027-12-31
Marketing Start 2005-08-06

Pharmacologic Class

Established (EPC)
expectorant [epc]
Physiologic Effect
decreased respiratory secretion viscosity [pe] increased respiratory secretions [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 03635027
Hyphenated Format 0363-5027

Supplemental Identifiers

RxCUI
1243679
UPC
0311917103723
UNII
362O9ITL9D 495W7451VQ 04JA59TNSJ
NUI
N0000193956 N0000008867 N0000009560

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 severe sinus daytime, non-drowsy (source: ndc)
Generic Name acetaminophen, guaifenesin, phenylephrine hcl (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 325 mg/1
  • 200 mg/1
  • 5 mg/1
source: ndc
Packaging
  • 2 BLISTER PACK in 1 CARTON (0363-5027-08) / 12 TABLET, FILM COATED in 1 BLISTER PACK
source: ndc

Packages (1)

0363-5027-08 2 BLISTER PACK in 1 CARTON (0363-5027-08) / 12 TABLET, FILM COATED in 1 BLISTER PACK

Ingredients (3)

acetaminophen (325 mg/1) guaifenesin (200 mg/1) phenylephrine hydrochloride (5 mg/1)

Linked Drug Pages (1)

Severe Sinus Daytime, Non-Drowsy ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "d8d12628-e9e4-4ab8-be43-1ef1538eeca3", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0311917103723"], "unii": ["362O9ITL9D", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1243679"], "spl_set_id": ["cc0dc951-5024-4517-9d38-a01699407e7e"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Walgreen Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (0363-5027-08)  / 12 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0363-5027-08", "marketing_start_date": "20050806"}], "brand_name": "Severe Sinus Daytime, Non-Drowsy", "product_id": "0363-5027_d8d12628-e9e4-4ab8-be43-1ef1538eeca3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "0363-5027", "generic_name": "Acetaminophen, Guaifenesin, Phenylephrine HCl", "labeler_name": "Walgreen Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Severe Sinus", "brand_name_suffix": "Daytime, Non-Drowsy", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "GUAIFENESIN", "strength": "200 mg/1"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20050806", "listing_expiration_date": "20271231"}