daytime, nighttime severe cold and flu relief

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

Labeler: cvs woonsocket prescription center, incorporated
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name daytime, nighttime severe cold and flu relief
Generic Name acetaminophen, dextromethorphan hbr, doxylamine succinate, guaifenesin, phenylephrine hcl
Labeler cvs woonsocket prescription center, incorporated
Dosage Form KIT
Manufacturer
CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED

Identifiers & Regulatory

Product NDC 51316-647
Product ID 51316-647_d541ff04-1e02-4090-b22b-6417da4e3b39
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2022-11-03

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 51316647
Hyphenated Format 51316-647

Supplemental Identifiers

RxCUI
1110988 1546881 2634817
UPC
0050428547236

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, nighttime severe cold and flu relief (source: ndc)
Generic Name acetaminophen, dextromethorphan hbr, doxylamine succinate, guaifenesin, 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 (51316-647-22) * 8 TABLET, FILM COATED in 1 BLISTER PACK * 8 TABLET, FILM COATED in 1 BLISTER PACK
source: ndc

Packages (1)

51316-647-22 1 KIT in 1 CARTON (51316-647-22) * 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, Nighttime Severe Cold and Flu Relief ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "d541ff04-1e02-4090-b22b-6417da4e3b39", "openfda": {"upc": ["0050428547236"], "rxcui": ["1110988", "1546881", "2634817"], "spl_set_id": ["c3b7fab1-f7fe-41be-a1c4-7ba4ba23c159"], "manufacturer_name": ["CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (51316-647-22)  *  8 TABLET, FILM COATED in 1 BLISTER PACK *  8 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "51316-647-22", "marketing_start_date": "20221103"}], "brand_name": "Daytime, Nighttime Severe Cold and Flu Relief", "product_id": "51316-647_d541ff04-1e02-4090-b22b-6417da4e3b39", "dosage_form": "KIT", "product_ndc": "51316-647", "generic_name": "Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, Guaifenesin, Phenylephrine HCl", "labeler_name": "CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Daytime, Nighttime Severe Cold and Flu Relief", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20221103", "listing_expiration_date": "20261231"}