mucinex nightshift sinus maximum strength

Generic: acetaminophen, dextromethorphan hydrobromide, and triprolidine hydrochloride

Labeler: rb health (us) llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name mucinex nightshift sinus maximum strength
Generic Name acetaminophen, dextromethorphan hydrobromide, and triprolidine hydrochloride
Labeler rb health (us) llc
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

acetaminophen 325 mg/1, dextromethorphan hydrobromide 10 mg/1, triprolidine hydrochloride 1.25 mg/1

Manufacturer
RB Health (US) LLC

Identifiers & Regulatory

Product NDC 72854-209
Product ID 72854-209_35322ca5-3819-1ec8-e063-6394a90a262f
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2025-05-01

Pharmacologic Class

Classes
sigma-1 agonist [epc] sigma-1 receptor agonists [moa] uncompetitive n-methyl-d-aspartate receptor antagonist [epc] uncompetitive nmda receptor antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72854209
Hyphenated Format 72854-209

Supplemental Identifiers

RxCUI
2549034
UPC
0363824999364
UNII
362O9ITL9D 9D2RTI9KYH YAN7R5L890

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 mucinex nightshift sinus maximum strength (source: ndc)
Generic Name acetaminophen, dextromethorphan hydrobromide, and triprolidine hydrochloride (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 325 mg/1
  • 10 mg/1
  • 1.25 mg/1
source: ndc
Packaging
  • 2 BLISTER PACK in 1 CARTON (72854-209-20) / 10 TABLET, COATED in 1 BLISTER PACK
source: ndc

Packages (1)

72854-209-20 2 BLISTER PACK in 1 CARTON (72854-209-20) / 10 TABLET, COATED in 1 BLISTER PACK

Ingredients (3)

acetaminophen (325 mg/1) dextromethorphan hydrobromide (10 mg/1) triprolidine hydrochloride (1.25 mg/1)

Linked Drug Pages (1)

Mucinex Nightshift Sinus Maximum Strength ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "35322ca5-3819-1ec8-e063-6394a90a262f", "openfda": {"upc": ["0363824999364"], "unii": ["362O9ITL9D", "9D2RTI9KYH", "YAN7R5L890"], "rxcui": ["2549034"], "spl_set_id": ["35322238-d498-1a52-e063-6394a90ac9c4"], "manufacturer_name": ["RB Health (US) LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (72854-209-20)  / 10 TABLET, COATED in 1 BLISTER PACK", "package_ndc": "72854-209-20", "marketing_start_date": "20250501"}], "brand_name": "Mucinex Nightshift Sinus Maximum Strength", "product_id": "72854-209_35322ca5-3819-1ec8-e063-6394a90a262f", "dosage_form": "TABLET, COATED", "pharm_class": ["Sigma-1 Agonist [EPC]", "Sigma-1 Receptor Agonists [MoA]", "Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]", "Uncompetitive NMDA Receptor Antagonists [MoA]"], "product_ndc": "72854-209", "generic_name": "Acetaminophen, Dextromethorphan Hydrobromide, and Triprolidine Hydrochloride", "labeler_name": "RB Health (US) LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucinex Nightshift Sinus", "brand_name_suffix": "Maximum Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "10 mg/1"}, {"name": "TRIPROLIDINE HYDROCHLORIDE", "strength": "1.25 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250501", "listing_expiration_date": "20261231"}