daytime cold and flu nitetime cold and flu

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

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

Drug Facts

Product Profile

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

Identifiers & Regulatory

Product NDC 41250-919
Product ID 41250-919_c0a60075-c87f-4dee-a9d2-58c39bf8ab78
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2019-03-29

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 41250919
Hyphenated Format 41250-919

Supplemental Identifiers

RxCUI
1369842 1431245 2637731

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 nitetime cold and flu (source: ndc)
Generic Name acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, guaifenesin, phenylephrine hydrochloride (source: ndc)
Application Number M012 (source: ndc)

Resolved Composition

Strengths
  • 30 ml
  • 650 mg
  • 20 mg
  • 12.5 mg
  • 10 mg
  • 15 ml
  • 325 mg
  • 200 mg
  • 5 mg
source: label
Packaging
  • 1 KIT in 1 CARTON (41250-919-02) * 355 mL in 1 BOTTLE (41250-603-40) * 355 mL in 1 BOTTLE (41250-811-40)
source: ndc

Packages (1)

41250-919-02 1 KIT in 1 CARTON (41250-919-02) * 355 mL in 1 BOTTLE (41250-603-40) * 355 mL in 1 BOTTLE (41250-811-40)

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

DAYTIME COLD AND FLU NITETIME COLD AND FLU ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "c0a60075-c87f-4dee-a9d2-58c39bf8ab78", "openfda": {"rxcui": ["1369842", "1431245", "2637731"], "spl_set_id": ["3a33c6ce-aada-4099-8c61-49c86c0fc1a8"], "manufacturer_name": ["Meijer Distribution Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (41250-919-02)  *  355 mL in 1 BOTTLE (41250-603-40)  *  355 mL in 1 BOTTLE (41250-811-40)", "package_ndc": "41250-919-02", "marketing_start_date": "20190329"}], "brand_name": "DAYTIME COLD AND FLU NITETIME COLD AND FLU", "product_id": "41250-919_c0a60075-c87f-4dee-a9d2-58c39bf8ab78", "dosage_form": "KIT", "product_ndc": "41250-919", "generic_name": "acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, guaifenesin, phenylephrine hydrochloride", "labeler_name": "Meijer Distribution Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "DAYTIME COLD AND FLU NITETIME COLD AND FLU", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190329", "listing_expiration_date": "20261231"}