mucinex nightshift severe cold and flu maximum strength

Generic: acetaminophen, dextromethorphan hydrobromide, phenylephrine hydrochloride, 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 severe cold and flu maximum strength
Generic Name acetaminophen, dextromethorphan hydrobromide, phenylephrine hydrochloride, 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, phenylephrine hydrochloride 5 mg/1, triprolidine hydrochloride 1.25 mg/1

Manufacturer
RB Health (US) LLC

Identifiers & Regulatory

Product NDC 72854-234
Product ID 72854-234_07621dc9-9ae8-1c1e-e063-6294a90a88f3
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2021-07-01

Pharmacologic Class

Classes
adrenergic alpha1-agonists [moa] sigma-1 agonist [epc] sigma-1 receptor agonists [moa] uncompetitive n-methyl-d-aspartate receptor antagonist [epc] uncompetitive nmda receptor antagonists [moa] alpha-1 adrenergic agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72854234
Hyphenated Format 72854-234

Supplemental Identifiers

RxCUI
2549037
UNII
362O9ITL9D 9D2RTI9KYH 04JA59TNSJ 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 severe cold and flu maximum strength (source: ndc)
Generic Name acetaminophen, dextromethorphan hydrobromide, phenylephrine hydrochloride, and triprolidine hydrochloride (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 325 mg/1
  • 10 mg/1
  • 5 mg/1
  • 1.25 mg/1
source: ndc
Packaging
  • 2 TABLET, COATED in 1 PACKET (72854-234-02)
  • 2 BLISTER PACK in 1 CARTON (72854-234-20) / 10 TABLET, COATED in 1 BLISTER PACK
source: ndc

Packages (2)

72854-234-02 2 TABLET, COATED in 1 PACKET (72854-234-02) 72854-234-20 2 BLISTER PACK in 1 CARTON (72854-234-20) / 10 TABLET, COATED in 1 BLISTER PACK

Ingredients (4)

acetaminophen (325 mg/1) dextromethorphan hydrobromide (10 mg/1) phenylephrine hydrochloride (5 mg/1) triprolidine hydrochloride (1.25 mg/1)

Linked Drug Pages (1)

Mucinex Nightshift Severe Cold and Flu Maximum Strength ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "07621dc9-9ae8-1c1e-e063-6294a90a88f3", "openfda": {"unii": ["362O9ITL9D", "9D2RTI9KYH", "04JA59TNSJ", "YAN7R5L890"], "rxcui": ["2549037"], "spl_set_id": ["12420092-3ef6-464b-9106-2d56cd6ef200"], "manufacturer_name": ["RB Health (US) LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": true, "description": "2 TABLET, COATED in 1 PACKET (72854-234-02)", "package_ndc": "72854-234-02", "marketing_start_date": "20210701"}, {"sample": false, "description": "2 BLISTER PACK in 1 CARTON (72854-234-20)  / 10 TABLET, COATED in 1 BLISTER PACK", "package_ndc": "72854-234-20", "marketing_start_date": "20210701"}], "brand_name": "Mucinex Nightshift Severe Cold and Flu Maximum Strength", "product_id": "72854-234_07621dc9-9ae8-1c1e-e063-6294a90a88f3", "dosage_form": "TABLET, COATED", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Sigma-1 Agonist [EPC]", "Sigma-1 Receptor Agonists [MoA]", "Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]", "Uncompetitive NMDA Receptor Antagonists [MoA]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "72854-234", "generic_name": "Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride, and Triprolidine Hydrochloride", "labeler_name": "RB Health (US) LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucinex Nightshift Severe Cold and Flu", "brand_name_suffix": "Maximum Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "10 mg/1"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "5 mg/1"}, {"name": "TRIPROLIDINE HYDROCHLORIDE", "strength": "1.25 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210701", "listing_expiration_date": "20261231"}