theraflu severe cold relief daytime berry burst

Generic: acetaminophen, dextromethorphan hbr

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

Drug Facts

Product Profile

Brand Name theraflu severe cold relief daytime berry burst
Generic Name acetaminophen, dextromethorphan hbr
Labeler haleon us holdings llc
Dosage Form POWDER, FOR SOLUTION
Routes
ORAL
Active Ingredients

acetaminophen 650 mg/1, dextromethorphan hydrobromide 20 mg/1

Manufacturer
Haleon US Holdings LLC

Identifiers & Regulatory

Product NDC 0067-0106
Product ID 0067-0106_132dee3d-4a55-2c83-e063-6294a90a6729
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2023-12-01

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 00670106
Hyphenated Format 0067-0106

Supplemental Identifiers

RxCUI
2670678
UNII
362O9ITL9D 9D2RTI9KYH

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 severe cold relief daytime berry burst (source: ndc)
Generic Name acetaminophen, dextromethorphan hbr (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 650 mg/1
  • 20 mg/1
source: ndc
Packaging
  • 6 PACKET in 1 CARTON (0067-0106-06) / 1 POWDER, FOR SOLUTION in 1 PACKET
source: ndc

Packages (1)

0067-0106-06 6 PACKET in 1 CARTON (0067-0106-06) / 1 POWDER, FOR SOLUTION in 1 PACKET

Ingredients (2)

acetaminophen (650 mg/1) dextromethorphan hydrobromide (20 mg/1)

Linked Drug Pages (1)

Theraflu Severe Cold Relief Daytime Berry Burst ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "132dee3d-4a55-2c83-e063-6294a90a6729", "openfda": {"unii": ["362O9ITL9D", "9D2RTI9KYH"], "rxcui": ["2670678"], "spl_set_id": ["adf33520-4689-4de2-b9d8-c201518e9d26"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 PACKET in 1 CARTON (0067-0106-06)  / 1 POWDER, FOR SOLUTION in 1 PACKET", "package_ndc": "0067-0106-06", "marketing_start_date": "20231201"}], "brand_name": "Theraflu Severe Cold Relief Daytime Berry Burst", "product_id": "0067-0106_132dee3d-4a55-2c83-e063-6294a90a6729", "dosage_form": "POWDER, FOR SOLUTION", "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": "0067-0106", "generic_name": "ACETAMINOPHEN, DEXTROMETHORPHAN HBr", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Theraflu Severe Cold Relief Daytime Berry Burst", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/1"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "20 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20231201", "listing_expiration_date": "20261231"}