cold relief multi-symptom
Generic: acetaminophen, dextromethorphan hbr, phenylephrine hcl
Labeler: cardinal health 110, llc. dba leaderDrug Facts
Product Profile
Brand Name
cold relief multi-symptom
Generic Name
acetaminophen, dextromethorphan hbr, phenylephrine hcl
Labeler
cardinal health 110, llc. dba leader
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
acetaminophen 325 mg/1, dextromethorphan hydrobromide 10 mg/1, phenylephrine hydrochloride 5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70000-0652
Product ID
70000-0652_fce92425-b840-4c82-9597-39da622dedc4
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M012
Listing Expiration
2026-12-31
Marketing Start
2023-10-25
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
700000652
Hyphenated Format
70000-0652
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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
cold relief multi-symptom (source: ndc)
Generic Name
acetaminophen, dextromethorphan hbr, phenylephrine hcl (source: ndc)
Application Number
M012 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 325 mg/1
- 10 mg/1
- 5 mg/1
Packaging
- 2 BLISTER PACK in 1 CARTON (70000-0652-1) / 12 TABLET, FILM COATED in 1 BLISTER PACK
Packages (1)
Ingredients (3)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "fce92425-b840-4c82-9597-39da622dedc4", "openfda": {"upc": ["0096295143027"], "unii": ["362O9ITL9D", "9D2RTI9KYH", "04JA59TNSJ"], "rxcui": ["1094538"], "spl_set_id": ["0c94780d-e901-43fc-ad8a-80c5d61ea47b"], "manufacturer_name": ["Cardinal Health 110, LLC. DBA Leader"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (70000-0652-1) / 12 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "70000-0652-1", "marketing_start_date": "20231025"}], "brand_name": "Cold Relief Multi-Symptom", "product_id": "70000-0652_fce92425-b840-4c82-9597-39da622dedc4", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Sigma-1 Agonist [EPC]", "Sigma-1 Receptor Agonists [MoA]", "Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]", "Uncompetitive NMDA Receptor Antagonists [MoA]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "70000-0652", "generic_name": "Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl", "labeler_name": "Cardinal Health 110, LLC. DBA Leader", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cold Relief", "brand_name_suffix": "Multi-Symptom", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "10 mg/1"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20231025", "listing_expiration_date": "20261231"}