theraflu-d flu relief max strength plus nasal decongestant nighttime

Generic: acetaminophen, chlorpheniramine maleate, dextromethorphan hbr, pseudoephedrine hcl

Labeler: haleon us holdings llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name theraflu-d flu relief max strength plus nasal decongestant nighttime
Generic Name acetaminophen, chlorpheniramine maleate, dextromethorphan hbr, pseudoephedrine hcl
Labeler haleon us holdings llc
Dosage Form SYRUP
Routes
ORAL
Active Ingredients

acetaminophen 1000 mg/30mL, chlorpheniramine maleate 4 mg/30mL, dextromethorphan hydrobromide 30 mg/30mL, pseudoephedrine hydrochloride 60 mg/30mL

Manufacturer
Haleon US Holdings LLC

Identifiers & Regulatory

Product NDC 0067-0114
Product ID 0067-0114_178e716d-ce9d-a6ca-e063-6294a90a4371
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2024-06-19

Pharmacologic Class

Classes
adrenergic alpha-agonists [moa] histamine h1 receptor antagonists [moa] histamine-1 receptor antagonist [epc] sigma-1 agonist [epc] sigma-1 receptor agonists [moa] uncompetitive n-methyl-d-aspartate receptor antagonist [epc] uncompetitive nmda receptor antagonists [moa] alpha-adrenergic agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 00670114
Hyphenated Format 0067-0114

Supplemental Identifiers

RxCUI
2049283
UNII
362O9ITL9D V1Q0O9OJ9Z 9D2RTI9KYH 6V9V2RYJ8N

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 theraflu-d flu relief max strength plus nasal decongestant nighttime (source: ndc)
Generic Name acetaminophen, chlorpheniramine maleate, dextromethorphan hbr, pseudoephedrine hcl (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1000 mg/30mL
  • 4 mg/30mL
  • 30 mg/30mL
  • 60 mg/30mL
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (0067-0114-01) / 237 mL in 1 BOTTLE
source: ndc

Packages (1)

Ingredients (4)

acetaminophen (1000 mg/30mL) chlorpheniramine maleate (4 mg/30mL) dextromethorphan hydrobromide (30 mg/30mL) pseudoephedrine hydrochloride (60 mg/30mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "178e716d-ce9d-a6ca-e063-6294a90a4371", "openfda": {"unii": ["362O9ITL9D", "V1Q0O9OJ9Z", "9D2RTI9KYH", "6V9V2RYJ8N"], "rxcui": ["2049283"], "spl_set_id": ["09e20842-2b75-43b9-ae5f-3515b35e655b"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0067-0114-01)  / 237 mL in 1 BOTTLE", "package_ndc": "0067-0114-01", "marketing_start_date": "20240619"}], "brand_name": "Theraflu-D Flu Relief Max Strength plus Nasal Decongestant Nighttime", "product_id": "0067-0114_178e716d-ce9d-a6ca-e063-6294a90a4371", "dosage_form": "SYRUP", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]", "Sigma-1 Agonist [EPC]", "Sigma-1 Receptor Agonists [MoA]", "Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]", "Uncompetitive NMDA Receptor Antagonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "0067-0114", "generic_name": "Acetaminophen, Chlorpheniramine maleate, Dextromethorphan HBr, Pseudoephedrine HCl", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Theraflu-D Flu Relief Max Strength plus Nasal Decongestant", "brand_name_suffix": "Nighttime", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "1000 mg/30mL"}, {"name": "CHLORPHENIRAMINE MALEATE", "strength": "4 mg/30mL"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "30 mg/30mL"}, {"name": "PSEUDOEPHEDRINE HYDROCHLORIDE", "strength": "60 mg/30mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240619", "listing_expiration_date": "20261231"}