day and night sinus relief maximum strength

Generic: acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, guaifenesin, phenylephrine hydrochloride

Labeler: wal-mart stores, inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name day and night sinus relief maximum strength
Generic Name acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, guaifenesin, phenylephrine hydrochloride
Labeler wal-mart stores, inc.
Dosage Form KIT
Manufacturer
Wal-Mart Stores, Inc.

Identifiers & Regulatory

Product NDC 49035-587
Product ID 49035-587_2778ad80-7464-70e4-e063-6394a90a04f6
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2018-01-31

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 49035587
Hyphenated Format 49035-587

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 day and night sinus relief maximum strength (source: ndc)
Generic Name acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, guaifenesin, phenylephrine hydrochloride (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 KIT in 1 CARTON (49035-587-04) * 2 BLISTER PACK in 1 CARTON / 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK * 1 BLISTER PACK in 1 CARTON / 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
source: ndc

Packages (1)

49035-587-04 1 KIT in 1 CARTON (49035-587-04) * 2 BLISTER PACK in 1 CARTON / 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK * 1 BLISTER PACK in 1 CARTON / 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Day and Night Sinus Relief Maximum Strength ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "2778ad80-7464-70e4-e063-6394a90a04f6", "openfda": {"rxcui": ["1297288", "1656815", "2634364"], "spl_set_id": ["4b554ce8-9a6a-444f-b5ea-63359bbc0653"], "manufacturer_name": ["Wal-Mart Stores, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (49035-587-04)  *  2 BLISTER PACK in 1 CARTON / 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK *  1 BLISTER PACK in 1 CARTON / 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK", "package_ndc": "49035-587-04", "marketing_start_date": "20180131"}], "brand_name": "Day and Night Sinus Relief Maximum Strength", "product_id": "49035-587_2778ad80-7464-70e4-e063-6394a90a04f6", "dosage_form": "KIT", "product_ndc": "49035-587", "generic_name": "acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, guaifenesin, phenylephrine hydrochloride", "labeler_name": "Wal-Mart Stores, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Day and Night Sinus Relief", "brand_name_suffix": "Maximum Strength", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20180131", "listing_expiration_date": "20261231"}