theraflu relief max strength daytime

Generic: acetaminophen, dextromethorphan hbr

Labeler: cvs pharmacy
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name theraflu relief max strength daytime
Generic Name acetaminophen, dextromethorphan hbr
Labeler cvs pharmacy
Dosage Form POWDER, FOR SOLUTION
Routes
ORAL
Active Ingredients

acetaminophen 1000 mg/1, dextromethorphan hydrobromide 30 mg/1

Manufacturer
CVS PHARMACY

Identifiers & Regulatory

Product NDC 51316-539
Product ID 51316-539_456f2b31-da6f-baaa-e063-6394a90a8454
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2023-04-17

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 51316539
Hyphenated Format 51316-539

Supplemental Identifiers

RxCUI
2636656
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 relief max strength daytime (source: ndc)
Generic Name acetaminophen, dextromethorphan hbr (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1000 mg/1
  • 30 mg/1
source: ndc
Packaging
  • 1 POWDER, FOR SOLUTION in 1 PACKET (51316-539-06)
source: ndc

Packages (1)

51316-539-06 1 POWDER, FOR SOLUTION in 1 PACKET (51316-539-06)

Ingredients (2)

acetaminophen (1000 mg/1) dextromethorphan hydrobromide (30 mg/1)

Linked Drug Pages (1)

Theraflu Relief Max Strength Daytime ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "456f2b31-da6f-baaa-e063-6394a90a8454", "openfda": {"unii": ["362O9ITL9D", "9D2RTI9KYH"], "rxcui": ["2636656"], "spl_set_id": ["932a3d40-9b52-4e91-bc61-6fd506f2d9e6"], "manufacturer_name": ["CVS PHARMACY"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 POWDER, FOR SOLUTION in 1 PACKET (51316-539-06)", "package_ndc": "51316-539-06", "marketing_start_date": "20230417"}], "brand_name": "Theraflu Relief Max Strength Daytime", "product_id": "51316-539_456f2b31-da6f-baaa-e063-6394a90a8454", "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": "51316-539", "generic_name": "Acetaminophen, Dextromethorphan HBr", "labeler_name": "CVS PHARMACY", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Theraflu Relief Max Strength", "brand_name_suffix": "Daytime", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "1000 mg/1"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "30 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230417", "listing_expiration_date": "20261231"}