daytime nighttime sinus relief maximum strength

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

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

Drug Facts

Product Profile

Brand Name daytime nighttime sinus relief maximum strength
Generic Name acetaminophen, dextromethorphan hbr, doxylamine succinate, phenylephrine hcl,guaifenesin
Labeler cvs pharmacy
Dosage Form KIT
Routes
ORAL
Manufacturer
CVS Pharmacy

Identifiers & Regulatory

Product NDC 69842-908
Product ID 69842-908_7063a29b-2389-4586-983b-e7314097488a
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Marketing Start 2019-10-30
Marketing End 2026-12-30

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69842908
Hyphenated Format 69842-908

Supplemental Identifiers

RxCUI
1297288 1656815 2634364
UPC
0050428546611

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 sinus relief maximum strength (source: ndc)
Generic Name acetaminophen, dextromethorphan hbr, doxylamine succinate, phenylephrine hcl,guaifenesin (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 325 mg
  • 10 mg
  • 200 mg
  • 5 mg
  • 6.25 mg
source: label
Packaging
  • 1 KIT in 1 KIT (69842-908-24) * 16 BLISTER PACK in 1 CARTON / 1 CAPSULE in 1 BLISTER PACK * 8 BLISTER PACK in 1 CARTON / 1 CAPSULE in 1 BLISTER PACK
source: ndc

Packages (1)

69842-908-24 1 KIT in 1 KIT (69842-908-24) * 16 BLISTER PACK in 1 CARTON / 1 CAPSULE in 1 BLISTER PACK * 8 BLISTER PACK in 1 CARTON / 1 CAPSULE in 1 BLISTER PACK

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Daytime Nighttime Sinus Relief Maximum Strength ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "7063a29b-2389-4586-983b-e7314097488a", "openfda": {"upc": ["0050428546611"], "rxcui": ["1297288", "1656815", "2634364"], "spl_set_id": ["1de2a7fd-129e-4b7b-a9bf-7a5811367bbf"], "manufacturer_name": ["CVS Pharmacy"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 KIT (69842-908-24)  *  16 BLISTER PACK in 1 CARTON / 1 CAPSULE in 1 BLISTER PACK *  8 BLISTER PACK in 1 CARTON / 1 CAPSULE in 1 BLISTER PACK", "package_ndc": "69842-908-24", "marketing_end_date": "20261230", "marketing_start_date": "20191030"}], "brand_name": "Daytime Nighttime Sinus Relief Maximum Strength", "product_id": "69842-908_7063a29b-2389-4586-983b-e7314097488a", "dosage_form": "KIT", "product_ndc": "69842-908", "generic_name": "Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, Phenylephrine HCL,Guaifenesin", "labeler_name": "CVS Pharmacy", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Daytime Nighttime Sinus Relief", "brand_name_suffix": "Maximum Strength", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20261230", "marketing_start_date": "20191030"}