daytime cold and flu nighttime cold and flu

Generic: acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, doxylamine succinate

Labeler: meijer, inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name daytime cold and flu nighttime cold and flu
Generic Name acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, doxylamine succinate
Labeler meijer, inc.
Dosage Form KIT
Manufacturer
Meijer, Inc.

Identifiers & Regulatory

Product NDC 79481-5200
Product ID 79481-5200_f857f8f6-75d6-464c-b305-48df7387e875
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2021-08-21

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 794815200
Hyphenated Format 79481-5200

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 daytime cold and flu nighttime cold and flu (source: ndc)
Generic Name acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, doxylamine succinate (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 CARTON (79481-5200-0) * 2 TABLET, FILM COATED in 1 BLISTER PACK (41250-569-00) * 2 TABLET, FILM COATED in 1 BLISTER PACK (79481-0099-0)
source: ndc

Packages (1)

79481-5200-0 1 KIT in 1 CARTON (79481-5200-0) * 2 TABLET, FILM COATED in 1 BLISTER PACK (41250-569-00) * 2 TABLET, FILM COATED in 1 BLISTER PACK (79481-0099-0)

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

daytime cold and flu nighttime cold and flu ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "f857f8f6-75d6-464c-b305-48df7387e875", "openfda": {"rxcui": ["1110988", "1546881", "2634817"], "spl_set_id": ["df31056b-d0eb-4094-98d9-3d444210d50d"], "manufacturer_name": ["Meijer, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (79481-5200-0)  *  2 TABLET, FILM COATED in 1 BLISTER PACK (41250-569-00)  *  2 TABLET, FILM COATED in 1 BLISTER PACK (79481-0099-0)", "package_ndc": "79481-5200-0", "marketing_start_date": "20210821"}], "brand_name": "daytime cold and flu nighttime cold and flu", "product_id": "79481-5200_f857f8f6-75d6-464c-b305-48df7387e875", "dosage_form": "KIT", "product_ndc": "79481-5200", "generic_name": "acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, doxylamine succinate", "labeler_name": "Meijer, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "daytime cold and flu nighttime cold and flu", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210821", "listing_expiration_date": "20261231"}