sinus pressure and pain daytime nighttime maximum strength

Generic: acetaminophen, diphenhydramine hcl, guaifenesin, phenylephrine hcl

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

Drug Facts

Product Profile

Brand Name sinus pressure and pain daytime nighttime maximum strength
Generic Name acetaminophen, diphenhydramine hcl, guaifenesin, phenylephrine hcl
Labeler walgreen company
Dosage Form KIT
Manufacturer
Walgreen Company

Identifiers & Regulatory

Product NDC 0363-6156
Product ID 0363-6156_69f0bd7c-7121-457e-a6d6-683ba81b711e
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2018-06-02

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 03636156
Hyphenated Format 0363-6156

Supplemental Identifiers

RxCUI
1233575 1243679 2634398

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 pressure and pain daytime nighttime maximum strength (source: ndc)
Generic Name acetaminophen, diphenhydramine hcl, guaifenesin, phenylephrine hcl (source: ndc)
Application Number M012 (source: ndc)

Resolved Composition

Strengths
  • 325 mg
  • 200 mg
  • 5 mg
  • 12.5 mg
source: label
Packaging
  • 1 KIT in 1 CARTON (0363-6156-10) * 12 TABLET, FILM COATED in 1 BLISTER PACK * 8 TABLET, FILM COATED in 1 BLISTER PACK
source: ndc

Packages (1)

0363-6156-10 1 KIT in 1 CARTON (0363-6156-10) * 12 TABLET, FILM COATED in 1 BLISTER PACK * 8 TABLET, FILM COATED in 1 BLISTER PACK

Ingredients (0)

No ingredient records.

Linked Drug Pages (2)

Sinus Pressure and Pain Daytime Nighttime Maximum Strength ndc-match (0.9) Sinus Pressure and Pain Daytime Nighttime Maximum Strength ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "69f0bd7c-7121-457e-a6d6-683ba81b711e", "openfda": {"rxcui": ["1233575", "1243679", "2634398"], "spl_set_id": ["8647c136-a323-453a-8f57-e66938bbf639"], "manufacturer_name": ["Walgreen Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (0363-6156-10)  *  12 TABLET, FILM COATED in 1 BLISTER PACK *  8 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0363-6156-10", "marketing_start_date": "20180602"}], "brand_name": "Sinus Pressure and Pain Daytime Nighttime Maximum Strength", "product_id": "0363-6156_69f0bd7c-7121-457e-a6d6-683ba81b711e", "dosage_form": "KIT", "product_ndc": "0363-6156", "generic_name": "Acetaminophen, Diphenhydramine HCl, Guaifenesin, Phenylephrine HCl", "labeler_name": "Walgreen Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sinus Pressure and Pain", "brand_name_suffix": "Daytime Nighttime Maximum Strength", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20180602", "listing_expiration_date": "20261231"}