cold and flu daytime, nighttime, maximum strength

Generic: acetaminophen, dextromethorphan hbr, doxylamine succinate, guaifenesin, phenylephrine hcl

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

Drug Facts

Product Profile

Brand Name cold and flu daytime, nighttime, maximum strength
Generic Name acetaminophen, dextromethorphan hbr, doxylamine succinate, guaifenesin, phenylephrine hcl
Labeler walgreen company
Dosage Form KIT
Manufacturer
Walgreen Company

Identifiers & Regulatory

Product NDC 0363-6406
Product ID 0363-6406_617fd9e4-7577-4f5d-8518-8d1a7e78176b
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2015-08-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 03636406
Hyphenated Format 0363-6406

Supplemental Identifiers

RxCUI
1110988 1546881 2634817

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 cold and flu daytime, nighttime, maximum strength (source: ndc)
Generic Name acetaminophen, dextromethorphan hbr, doxylamine succinate, guaifenesin, phenylephrine hcl (source: ndc)
Application Number M012 (source: ndc)

Resolved Composition

Strengths
  • 325 mg
  • 10 mg
  • 200 mg
  • 5 mg
  • 6.25 mg
source: label
Packaging
  • 1 KIT in 1 PACKAGE, COMBINATION (0363-6406-08) * 8 TABLET, FILM COATED in 1 BLISTER PACK * 8 TABLET, FILM COATED in 1 BLISTER PACK
source: ndc

Packages (1)

0363-6406-08 1 KIT in 1 PACKAGE, COMBINATION (0363-6406-08) * 8 TABLET, FILM COATED in 1 BLISTER PACK * 8 TABLET, FILM COATED in 1 BLISTER PACK

Ingredients (0)

No ingredient records.

Linked Drug Pages (2)

Cold and Flu Daytime, Nighttime, Maximum Strength ndc-match (0.9) Cold and Flu Daytime, Nighttime, Maximum Strength ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "617fd9e4-7577-4f5d-8518-8d1a7e78176b", "openfda": {"rxcui": ["1110988", "1546881", "2634817"], "spl_set_id": ["4d199dc7-253f-48fd-a77d-f8b10f724dd1"], "manufacturer_name": ["Walgreen Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 PACKAGE, COMBINATION (0363-6406-08)  *  8 TABLET, FILM COATED in 1 BLISTER PACK *  8 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0363-6406-08", "marketing_start_date": "20150801"}], "brand_name": "Cold and Flu Daytime, Nighttime, Maximum Strength", "product_id": "0363-6406_617fd9e4-7577-4f5d-8518-8d1a7e78176b", "dosage_form": "KIT", "product_ndc": "0363-6406", "generic_name": "Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, Guaifenesin, Phenylephrine HCl", "labeler_name": "Walgreen Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cold and Flu", "brand_name_suffix": "Daytime, Nighttime, Maximum Strength", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20150801", "listing_expiration_date": "20261231"}