maximum strength daytime nighttime cold and flu

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

Labeler: cvs pharmacy, inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name maximum strength daytime nighttime cold and flu
Generic Name acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl acetaminophen, dextromethorphan hbr, doxylamine succinate, phenylephrine hcl
Labeler cvs pharmacy, inc.
Dosage Form KIT
Manufacturer
CVS Pharmacy, Inc.

Identifiers & Regulatory

Product NDC 69842-451
Product ID 69842-451_f20a8272-c2a6-3c69-e053-2a95a90a1c93
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2021-07-10

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69842451
Hyphenated Format 69842-451

Supplemental Identifiers

RxCUI
1297288 1656815 2634364
UPC
0050428298398

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 maximum strength daytime nighttime cold and flu (source: ndc)
Generic Name acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl acetaminophen, dextromethorphan hbr, 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 BLISTER PACK in 1 CARTON (69842-451-24) / 1 KIT in 1 BLISTER PACK * 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (69842-382-08) * 16 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (69842-094-16)
source: ndc

Packages (1)

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"spl_id": "f20a8272-c2a6-3c69-e053-2a95a90a1c93", "openfda": {"upc": ["0050428298398"], "rxcui": ["1297288", "1656815", "2634364"], "spl_set_id": ["c17b8f17-95f6-37e4-e053-2995a90a411a"], "manufacturer_name": ["CVS Pharmacy, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (69842-451-24)  / 1 KIT in 1 BLISTER PACK *  8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (69842-382-08)  *  16 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (69842-094-16)", "package_ndc": "69842-451-24", "marketing_start_date": "20210710"}], "brand_name": "MAXIMUM STRENGTH DAYTIME NIGHTTIME COLD AND FLU", "product_id": "69842-451_f20a8272-c2a6-3c69-e053-2a95a90a1c93", "dosage_form": "KIT", "product_ndc": "69842-451", "generic_name": "Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, Phenylephrine HCl", "labeler_name": "CVS Pharmacy, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "MAXIMUM STRENGTH DAYTIME NIGHTTIME COLD AND FLU", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210710", "listing_expiration_date": "20261231"}