maximum strength daytime nighttime sinus relief

Generic: acetaminophen dextromethorphan hbr guaifenesin phenylephrine hcl and 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 sinus relief
Generic Name acetaminophen dextromethorphan hbr guaifenesin phenylephrine hcl and acetaminophen dextromethorphan hbr doxylamine succinate phenylephrine hcl
Labeler cvs pharmacy, inc.
Dosage Form KIT
Manufacturer
CVS Pharmacy, Inc.

Identifiers & Regulatory

Product NDC 69842-442
Product ID 69842-442_f20a1beb-ceed-5e9e-e053-2a95a90a4e17
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 69842442
Hyphenated Format 69842-442

Supplemental Identifiers

RxCUI
1297288 1656815 2634364

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 sinus relief (source: ndc)
Generic Name acetaminophen dextromethorphan hbr guaifenesin phenylephrine hcl and 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 (69842-442-24) / 1 KIT in 1 BLISTER PACK * 16 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (69842-617-16) * 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (69842-290-08)
source: ndc

Packages (1)

69842-442-24 1 BLISTER PACK in 1 CARTON (69842-442-24) / 1 KIT in 1 BLISTER PACK * 16 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (69842-617-16) * 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (69842-290-08)

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

MAXIMUM STRENGTH DAYTIME NIGHTTIME SINUS RELIEF ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "f20a1beb-ceed-5e9e-e053-2a95a90a4e17", "openfda": {"rxcui": ["1297288", "1656815", "2634364"], "spl_set_id": ["c17d5ba7-3302-7931-e053-2a95a90a5a6c"], "manufacturer_name": ["CVS Pharmacy, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (69842-442-24)  / 1 KIT in 1 BLISTER PACK *  16 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (69842-617-16)  *  8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (69842-290-08)", "package_ndc": "69842-442-24", "marketing_start_date": "20210710"}], "brand_name": "MAXIMUM STRENGTH DAYTIME NIGHTTIME SINUS RELIEF", "product_id": "69842-442_f20a1beb-ceed-5e9e-e053-2a95a90a4e17", "dosage_form": "KIT", "product_ndc": "69842-442", "generic_name": "Acetaminophen Dextromethorphan HBr Guaifenesin Phenylephrine HCl And Acetaminophen Dextromethorphan HBr Doxylamine Succinate Phenylephrine HCl", "labeler_name": "CVS Pharmacy, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "MAXIMUM STRENGTH DAYTIME NIGHTTIME SINUS RELIEF", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210710", "listing_expiration_date": "20261231"}