daytime nighttime sinus relief maximum strength

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

Labeler: walgreens
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, guaifenesin, phenylephrine hcl/acetaminophen, dextromethorphan hbr, doxylamine succinate,phenylephrine hcl
Labeler walgreens
Dosage Form KIT
Manufacturer
Walgreens

Identifiers & Regulatory

Product NDC 0363-0744
Product ID 0363-0744_f210305b-7d30-6550-e053-2a95a90a0f05
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2022-06-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 03630744
Hyphenated Format 0363-0744

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 daytime nighttime sinus relief maximum strength (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
  • 6.25 mg
  • 5 mg
  • 200 mg
source: label
Packaging
  • 3 BLISTER PACK in 1 CARTON (0363-0744-24) / 1 KIT in 1 BLISTER PACK * 4 CAPSULE in 1 BLISTER PACK * 8 CAPSULE in 1 BLISTER PACK
source: ndc

Packages (1)

0363-0744-24 3 BLISTER PACK in 1 CARTON (0363-0744-24) / 1 KIT in 1 BLISTER PACK * 4 CAPSULE in 1 BLISTER PACK * 8 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 
{"spl_id": "f210305b-7d30-6550-e053-2a95a90a0f05", "openfda": {"rxcui": ["1297288", "1656815", "2634364"], "spl_set_id": ["da046b01-707c-326a-e053-2995a90a0927"], "manufacturer_name": ["Walgreens"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 CARTON (0363-0744-24)  / 1 KIT in 1 BLISTER PACK *  4 CAPSULE in 1 BLISTER PACK *  8 CAPSULE in 1 BLISTER PACK", "package_ndc": "0363-0744-24", "marketing_start_date": "20220601"}], "brand_name": "Daytime Nighttime Sinus Relief Maximum Strength", "product_id": "0363-0744_f210305b-7d30-6550-e053-2a95a90a0f05", "dosage_form": "KIT", "product_ndc": "0363-0744", "generic_name": "Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl/Acetaminophen, Dextromethorphan HBr, Doxylamine succinate,Phenylephrine HCl", "labeler_name": "Walgreens", "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_start_date": "20220601", "listing_expiration_date": "20261231"}