NDC 0363-5027

Severe Sinus Daytime, Non-Drowsy

Acetaminophen, Guaifenesin, Phenylephrine Hcl

Severe Sinus Daytime, Non-Drowsy is a Oral Tablet, Film Coated in the Human Otc Drug category. It is labeled and distributed by Walgreen Company. The primary component is Acetaminophen; Guaifenesin; Phenylephrine Hydrochloride.

• Product ID: 0363-5027_02b86dd9-16ee-412b-874f-559b8af1024c
• NDC: 0363-5027
• Product Type: Human Otc Drug
• Proprietary Name: Severe Sinus Daytime, Non-Drowsy
• Generic Name: Acetaminophen, Guaifenesin, Phenylephrine Hcl
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 2005-08-06
• Marketing Category: OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
• Application Number: part341
• Labeler Name: Walgreen Company
• Substance Name: ACETAMINOPHEN; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
• Active Ingredient Strength: 325 mg/1; mg/1; mg/1
• Pharm Classes: Adrenergic alpha1-Agonists [MoA], Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], alpha-1 Adrenergic Agonist [EPC]
• NDC Exclude Flag: N
• Listing Certified Through: 2023-12-31

Packaging

NDC 0363-5027-07

3 BLISTER PACK in 1 CARTON (0363-5027-07) > 12 TABLET, FILM COATED in 1 BLISTER PACK

• Marketing Start Date: 2005-08-06
• Marketing End Date: 2023-04-07
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0363-5027-07 [00363502707]

Severe Sinus Daytime, Non-Drowsy TABLET, FILM COATED

• Marketing Category: OTC MONOGRAPH FINAL
• Application Number: part341
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2005-08-06

NDC 0363-5027-08 [00363502708]

Severe Sinus Daytime, Non-Drowsy TABLET, FILM COATED

• Marketing Category: OTC MONOGRAPH FINAL
• Application Number: part341
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2005-08-06

Drug Details

Active Ingredients

Ingredient	Strength
ACETAMINOPHEN	325 mg/1

OpenFDA Data

• SPL SET ID: cc0dc951-5024-4517-9d38-a01699407e7e
• Manufacturer:
  • Walgreen Company
• UNII:
  • 362O9ITL9D
  • 04JA59TNSJ
  • 495W7451VQ
• RxNorm Concept Unique ID - RxCUI:
  • 1243679

NDC Crossover Matching brand name "Severe Sinus Daytime, Non-Drowsy" or generic name "Acetaminophen, Guaifenesin, Phenylephrine Hcl"

NDC	Brand Name	Generic Name
0363-9527	Cold and Head Congestion	Acetaminophen, Guaifenesin, Phenylephrine HCl
0113-0145	Good Sense Mucus Relief	Acetaminophen, guaifenesin, phenylephrine HCl
0363-0628	Mucus Relief	Acetaminophen, Guaifenesin, Phenylephrine HCl
0363-3350	Mucus Relief	Acetaminophen, Guaifenesin, Phenylephrine HCl
0363-0156	Mucus Relief Severe Sinus Congestion	Acetaminophen, Guaifenesin, Phenylephrine HCl
0363-4120	Pressure plus Pain plus Mucus	Acetaminophen, Guaifenesin, Phenylephrine HCl
0363-5027	Severe Sinus	Acetaminophen, Guaifenesin, Phenylephrine HCl
0363-6150	Severe Sinus Congestion	Acetaminophen, Guaifenesin, Phenylephrine HCl
11822-5160	severe sinus congestion relief	Acetaminophen, Guaifenesin, Phenylephrine HCl
0363-6028	Sinus Pressure and Pain	Acetaminophen, Guaifenesin, Phenylephrine HCl
11673-628	Sinus Pressure and Pain Relief	acetaminophen, guaifenesin, phenylephrine HCl
0363-0478	Sinus Relief Severe Congestion	Acetaminophen, Guaifenesin, Phenylephrine HCl
11673-927	Sinus Severe	Acetaminophen, Guaifenesin, Phenylephrine HCl
0363-4121	Wal-Phed HEAD CONGESTION AND MUCUS	Acetaminophen, Guaifenesin, Phenylephrine HCl