daytime/nitetime severe cold and flu maximum strength

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

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

Drug Facts

Product Profile

Brand Name daytime/nitetime severe cold and flu maximum strength
Generic Name acetaminophen, dextromethorphan hbr, guaifenesin, doxylamine succinate, phenylephrine hcl
Labeler meijer distribution inc
Dosage Form KIT
Manufacturer
Meijer Distribution Inc

Identifiers & Regulatory

Product NDC 41250-840
Product ID 41250-840_f484f06a-4f3f-4e81-aef3-4730ec48659c
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2027-12-31
Marketing Start 2015-08-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 41250840
Hyphenated Format 41250-840

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/nitetime severe cold and flu maximum strength (source: ndc)
Generic Name acetaminophen, dextromethorphan hbr, guaifenesin, doxylamine succinate, 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 CARTON (41250-840-22) * 8 TABLET, FILM COATED in 1 BLISTER PACK * 8 TABLET, FILM COATED in 1 BLISTER PACK
source: ndc

Packages (1)

41250-840-22 1 KIT in 1 CARTON (41250-840-22) * 8 TABLET, FILM COATED in 1 BLISTER PACK * 8 TABLET, FILM COATED in 1 BLISTER PACK

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

DayTime/NiteTime Severe Cold and Flu Maximum Strength ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "f484f06a-4f3f-4e81-aef3-4730ec48659c", "openfda": {"rxcui": ["1110988", "1546881", "2634817"], "spl_set_id": ["d07112dd-27df-46cc-b7c3-af8ba7601d06"], "manufacturer_name": ["Meijer Distribution Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (41250-840-22)  *  8 TABLET, FILM COATED in 1 BLISTER PACK *  8 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "41250-840-22", "marketing_start_date": "20150801"}], "brand_name": "DayTime/NiteTime Severe Cold and Flu Maximum Strength", "product_id": "41250-840_f484f06a-4f3f-4e81-aef3-4730ec48659c", "dosage_form": "KIT", "product_ndc": "41250-840", "generic_name": "Acetaminophen, Dextromethorphan HBr, Guaifenesin, Doxylamine Succinate, Phenylephrine HCl", "labeler_name": "Meijer Distribution Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "DayTime/NiteTime Severe Cold and Flu", "brand_name_suffix": "Maximum Strength", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20150801", "listing_expiration_date": "20271231"}