maximum strength sinus relief day and night softgels - 24 ct

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

Labeler: topco associates llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name maximum strength sinus relief day and night softgels - 24 ct
Generic Name acetaminophen, dextromethorphan hydrobromide, guaifenesin, doxylamine succinate, phenylephrine hydrochloride
Labeler topco associates llc
Dosage Form KIT
Manufacturer
Topco Associates LLC

Identifiers & Regulatory

Product NDC 76162-679
Product ID 76162-679_f0b81a05-8273-48e7-9ad3-877d7da8c200
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2025-10-13

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 76162679
Hyphenated Format 76162-679

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 sinus relief day and night softgels - 24 ct (source: ndc)
Generic Name acetaminophen, dextromethorphan hydrobromide, guaifenesin, doxylamine succinate, 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 (76162-679-24) * 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK * 4 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
source: ndc

Packages (1)

76162-679-24 1 KIT in 1 CARTON (76162-679-24) * 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK * 4 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

MAXIMUM STRENGTH Sinus Relief Day and Night SOFTGELS - 24 ct ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "f0b81a05-8273-48e7-9ad3-877d7da8c200", "openfda": {"rxcui": ["1297288", "1656815", "2634364"], "spl_set_id": ["a7285fe0-5a5b-42c4-be47-9a07a2ba75e8"], "manufacturer_name": ["Topco Associates LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 CARTON (76162-679-24)  *  8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK *  4 CAPSULE, LIQUID FILLED in 1 BLISTER PACK", "package_ndc": "76162-679-24", "marketing_start_date": "20251013"}], "brand_name": "MAXIMUM STRENGTH Sinus Relief Day and Night SOFTGELS - 24 ct", "product_id": "76162-679_f0b81a05-8273-48e7-9ad3-877d7da8c200", "dosage_form": "KIT", "product_ndc": "76162-679", "generic_name": "Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Doxylamine Succinate, Phenylephrine Hydrochloride", "labeler_name": "Topco Associates LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "MAXIMUM STRENGTH Sinus Relief Day and Night SOFTGELS - 24 ct", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20251013", "listing_expiration_date": "20261231"}