cold multi symptom daytime nighttime

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

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

Drug Facts

Product Profile

Brand Name cold multi symptom daytime nighttime
Generic Name acetaminophen, chlorpheniramine maleate, dextromethorphan hydrobromide, and phenylephrine hydrochloride
Labeler chain drug marketing association
Dosage Form KIT
Manufacturer
Chain Drug Marketing Association

Identifiers & Regulatory

Product NDC 63868-015
Product ID 63868-015_2889ede0-cc86-0dac-e063-6394a90a5a06
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2013-03-06

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63868015
Hyphenated Format 63868-015

Supplemental Identifiers

RxCUI
1086991 1094538 2634560
UPC
0635515969445

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 multi symptom daytime nighttime (source: ndc)
Generic Name acetaminophen, chlorpheniramine maleate, dextromethorphan hydrobromide, and phenylephrine hydrochloride (source: ndc)
Application Number M012 (source: ndc)

Resolved Composition

Strengths
  • 325 mg
  • 10 mg
  • 5 mg
  • 2 mg
source: label
Packaging
  • 1 KIT in 1 CARTON (63868-015-20) * 12 TABLET, COATED in 1 BLISTER PACK * 8 TABLET, COATED in 1 BLISTER PACK
source: ndc

Packages (1)

63868-015-20 1 KIT in 1 CARTON (63868-015-20) * 12 TABLET, COATED in 1 BLISTER PACK * 8 TABLET, COATED in 1 BLISTER PACK

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Cold Multi Symptom Daytime Nighttime ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "2889ede0-cc86-0dac-e063-6394a90a5a06", "openfda": {"upc": ["0635515969445"], "rxcui": ["1086991", "1094538", "2634560"], "spl_set_id": ["d5cbb5b0-564c-429e-b680-fa683e796393"], "manufacturer_name": ["Chain Drug Marketing Association"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (63868-015-20)  *  12 TABLET, COATED in 1 BLISTER PACK *  8 TABLET, COATED in 1 BLISTER PACK", "package_ndc": "63868-015-20", "marketing_start_date": "20130306"}], "brand_name": "Cold Multi Symptom Daytime Nighttime", "product_id": "63868-015_2889ede0-cc86-0dac-e063-6394a90a5a06", "dosage_form": "KIT", "product_ndc": "63868-015", "generic_name": "Acetaminophen, Chlorpheniramine Maleate, Dextromethorphan Hydrobromide, and Phenylephrine Hydrochloride", "labeler_name": "Chain Drug Marketing Association", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cold Multi Symptom Daytime Nighttime", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20130306", "listing_expiration_date": "20261231"}