theraflu relief max strength nighttime

Generic: acetaminophen, chlorpheniramine maleate and dextromethophan hbr

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

Drug Facts

Product Profile

Brand Name theraflu relief max strength nighttime
Generic Name acetaminophen, chlorpheniramine maleate and dextromethophan hbr
Labeler cvs pharmacy
Dosage Form POWDER, FOR SOLUTION
Routes
ORAL
Active Ingredients

acetaminophen 1000 mg/1, chlorpheniramine maleate 4 mg/1, dextromethorphan hydrobromide 30 mg/1

Manufacturer
CVS PHARMACY

Identifiers & Regulatory

Product NDC 51316-549
Product ID 51316-549_456f5b3a-842f-e145-e063-6394a90aa4d9
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M010
Listing Expiration 2026-12-31
Marketing Start 2023-04-17

Pharmacologic Class

Classes
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]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 51316549
Hyphenated Format 51316-549

Supplemental Identifiers

RxCUI
2636658
UNII
362O9ITL9D V1Q0O9OJ9Z 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 nighttime (source: ndc)
Generic Name acetaminophen, chlorpheniramine maleate and dextromethophan hbr (source: ndc)
Application Number M010 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1000 mg/1
  • 4 mg/1
  • 30 mg/1
source: ndc
Packaging
  • 1 POWDER, FOR SOLUTION in 1 PACKET (51316-549-06)
source: ndc

Packages (1)

51316-549-06 1 POWDER, FOR SOLUTION in 1 PACKET (51316-549-06)

Ingredients (3)

acetaminophen (1000 mg/1) chlorpheniramine maleate (4 mg/1) dextromethorphan hydrobromide (30 mg/1)

Linked Drug Pages (1)

Theraflu Relief Max Strength Nighttime ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "456f5b3a-842f-e145-e063-6394a90aa4d9", "openfda": {"unii": ["362O9ITL9D", "V1Q0O9OJ9Z", "9D2RTI9KYH"], "rxcui": ["2636658"], "spl_set_id": ["4b567234-1da9-4e10-a427-877eea2be1c1"], "manufacturer_name": ["CVS PHARMACY"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 POWDER, FOR SOLUTION in 1 PACKET (51316-549-06)", "package_ndc": "51316-549-06", "marketing_start_date": "20230417"}], "brand_name": "Theraflu Relief Max Strength Nighttime", "product_id": "51316-549_456f5b3a-842f-e145-e063-6394a90aa4d9", "dosage_form": "POWDER, FOR SOLUTION", "pharm_class": ["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]"], "product_ndc": "51316-549", "generic_name": "Acetaminophen, Chlorpheniramine Maleate and Dextromethophan HBr", "labeler_name": "CVS PHARMACY", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Theraflu Relief Max Strength", "brand_name_suffix": "Nighttime", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "1000 mg/1"}, {"name": "CHLORPHENIRAMINE MALEATE", "strength": "4 mg/1"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "30 mg/1"}], "application_number": "M010", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230417", "listing_expiration_date": "20261231"}