sinus severe daytime

Generic: acetaminophen, guaifenesin, phenylephrine hcl

Labeler: dolgencorp, llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name sinus severe daytime
Generic Name acetaminophen, guaifenesin, phenylephrine hcl
Labeler dolgencorp, llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

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

Manufacturer
DOLGENCORP, LLC

Identifiers & Regulatory

Product NDC 55910-529
Product ID 55910-529_850efbf9-ed31-45de-986b-bd69fb6de654
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
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 55910529
Hyphenated Format 55910-529

Supplemental Identifiers

RxCUI
1243679
UPC
0050844527089
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 sinus severe daytime (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 (55910-529-08) / 12 TABLET, FILM COATED in 1 BLISTER PACK
source: ndc

Packages (1)

55910-529-08 2 BLISTER PACK in 1 CARTON (55910-529-08) / 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)

Sinus Severe Daytime ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "850efbf9-ed31-45de-986b-bd69fb6de654", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0050844527089"], "unii": ["362O9ITL9D", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1243679"], "spl_set_id": ["b65baa7c-8197-4361-b3ef-e60eba38dca1"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["DOLGENCORP, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (55910-529-08)  / 12 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "55910-529-08", "marketing_start_date": "20050806"}], "brand_name": "Sinus Severe Daytime", "product_id": "55910-529_850efbf9-ed31-45de-986b-bd69fb6de654", "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": "55910-529", "generic_name": "Acetaminophen, Guaifenesin, Phenylephrine HCl", "labeler_name": "DOLGENCORP, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sinus Severe", "brand_name_suffix": "Daytime", "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": "20261231"}