cold and flu severe, daytime, nighttime

Generic: acetaminophen, chlorpheniramine maleate, dextromethorphan hbr, guaifenesin, phenylephrine hcl

Labeler: rite aid corporation
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name cold and flu severe, daytime, nighttime
Generic Name acetaminophen, chlorpheniramine maleate, dextromethorphan hbr, guaifenesin, phenylephrine hcl
Labeler rite aid corporation
Dosage Form KIT
Manufacturer
Rite Aid Corporation

Identifiers & Regulatory

Product NDC 11822-5034
Product ID 11822-5034_03173be8-37ae-45da-a689-2e7e9215282a
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2021-06-30

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 118225034
Hyphenated Format 11822-5034

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, daytime, nighttime (source: ndc)
Generic Name acetaminophen, chlorpheniramine maleate, dextromethorphan hbr, guaifenesin, phenylephrine hcl (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 (11822-5034-8) * 8 TABLET, FILM COATED in 1 BLISTER PACK (11822-5347-9) * 8 TABLET, FILM COATED in 1 BLISTER PACK (11822-4753-9)
source: ndc

Packages (1)

11822-5034-8 1 KIT in 1 CARTON (11822-5034-8) * 8 TABLET, FILM COATED in 1 BLISTER PACK (11822-5347-9) * 8 TABLET, FILM COATED in 1 BLISTER PACK (11822-4753-9)

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Cold and Flu Severe, Daytime, Nighttime ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "03173be8-37ae-45da-a689-2e7e9215282a", "openfda": {"rxcui": ["1086991", "1110988", "2634819"], "spl_set_id": ["a0bff310-2d35-4a18-815b-8386e44730a2"], "manufacturer_name": ["Rite Aid Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (11822-5034-8)  *  8 TABLET, FILM COATED in 1 BLISTER PACK (11822-5347-9)  *  8 TABLET, FILM COATED in 1 BLISTER PACK (11822-4753-9)", "package_ndc": "11822-5034-8", "marketing_start_date": "20210630"}], "brand_name": "Cold and Flu Severe, Daytime, Nighttime", "product_id": "11822-5034_03173be8-37ae-45da-a689-2e7e9215282a", "dosage_form": "KIT", "product_ndc": "11822-5034", "generic_name": "Acetaminophen, Chlorpheniramine maleate, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl", "labeler_name": "Rite Aid Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cold and Flu", "brand_name_suffix": "Severe, Daytime, Nighttime", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210630", "listing_expiration_date": "20261231"}