theraflu severe cold relief daytime

Generic: acetaminophen, dextromethorphan hbr

Labeler: r j general corporation
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name theraflu severe cold relief daytime
Generic Name acetaminophen, dextromethorphan hbr
Labeler r j general corporation
Dosage Form POWDER, FOR SOLUTION
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1, dextromethorphan hydrobromide 20 mg/1

Manufacturer
R J General Corporation

Identifiers & Regulatory

Product NDC 70264-047
Product ID 70264-047_43c91d3a-f1f9-ffcd-e063-6294a90a7860
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2024-11-12

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 70264047
Hyphenated Format 70264-047

Supplemental Identifiers

RxCUI
2670598
UNII
362O9ITL9D 9D2RTI9KYH

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 (source: ndc)
Generic Name acetaminophen, dextromethorphan hbr (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
  • 20 mg/1
source: ndc
Packaging
  • 25 PACKET in 1 CARTON (70264-047-01) / 1 POWDER, FOR SOLUTION in 1 PACKET
source: ndc

Packages (1)

70264-047-01 25 PACKET in 1 CARTON (70264-047-01) / 1 POWDER, FOR SOLUTION in 1 PACKET

Ingredients (2)

acetaminophen (500 mg/1) dextromethorphan hydrobromide (20 mg/1)

Linked Drug Pages (1)

Theraflu Severe Cold Relief Daytime ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "43c91d3a-f1f9-ffcd-e063-6294a90a7860", "openfda": {"unii": ["362O9ITL9D", "9D2RTI9KYH"], "rxcui": ["2670598"], "spl_set_id": ["8f0e4876-6bf0-4f6d-9cf0-f2aef2682ffc"], "manufacturer_name": ["R J General Corporation"]}, "finished": true, "packaging": [{"sample": false, "description": "25 PACKET in 1 CARTON (70264-047-01)  / 1 POWDER, FOR SOLUTION in 1 PACKET", "package_ndc": "70264-047-01", "marketing_start_date": "20241112"}], "brand_name": "Theraflu Severe Cold Relief Daytime", "product_id": "70264-047_43c91d3a-f1f9-ffcd-e063-6294a90a7860", "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": "70264-047", "generic_name": "ACETAMINOPHEN, DEXTROMETHORPHAN HBr", "labeler_name": "R J General Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Theraflu Severe Cold Relief Daytime", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/1"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "20 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20241112", "listing_expiration_date": "20261231"}