cold and flu severe day and night

Generic: acetaminophen, chlorpheniramine maleate, dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride

Labeler: chain drug marketing association, inc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name cold and flu severe day and night
Generic Name acetaminophen, chlorpheniramine maleate, dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride
Labeler chain drug marketing association, inc
Dosage Form KIT
Manufacturer
CHAIN DRUG MARKETING ASSOCIATION, INC

Identifiers & Regulatory

Product NDC 83324-092
Product ID 83324-092_1d8bb148-461a-3efa-e063-6394a90ad4fc
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2024-07-18

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 83324092
Hyphenated Format 83324-092

Supplemental Identifiers

RxCUI
1086991 1110988 2634819

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 severe day and night (source: ndc)
Generic Name acetaminophen, chlorpheniramine maleate, dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride (source: ndc)
Application Number M012 (source: ndc)

Resolved Composition

Strengths
  • 325 mg
  • 10 mg
  • 200 mg
  • 5 mg
  • 2 mg
source: label
Packaging
  • 1 KIT in 1 CARTON (83324-092-24) * 8 TABLET, COATED in 1 BLISTER PACK * 8 TABLET, COATED in 1 BLISTER PACK
source: ndc

Packages (1)

83324-092-24 1 KIT in 1 CARTON (83324-092-24) * 8 TABLET, COATED in 1 BLISTER PACK * 8 TABLET, COATED in 1 BLISTER PACK

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Cold and Flu Severe Day and Night ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "1d8bb148-461a-3efa-e063-6394a90ad4fc", "openfda": {"rxcui": ["1086991", "1110988", "2634819"], "spl_set_id": ["9b74dd00-8f84-4fce-b5ea-df886b595326"], "manufacturer_name": ["CHAIN DRUG MARKETING ASSOCIATION, INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (83324-092-24)  *  8 TABLET, COATED in 1 BLISTER PACK *  8 TABLET, COATED in 1 BLISTER PACK", "package_ndc": "83324-092-24", "marketing_start_date": "20240718"}], "brand_name": "Cold and Flu Severe Day and Night", "product_id": "83324-092_1d8bb148-461a-3efa-e063-6394a90ad4fc", "dosage_form": "KIT", "product_ndc": "83324-092", "generic_name": "Acetaminophen, Chlorpheniramine Maleate, Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride", "labeler_name": "CHAIN DRUG MARKETING ASSOCIATION, INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cold and Flu Severe Day and Night", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240718", "listing_expiration_date": "20261231"}