sanatos severe cold and cough daytime

Generic: acetaminophen, dextromethorphan hydrobromide, and phenylephrine hydrochloride

Labeler: pharmadel llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name sanatos severe cold and cough daytime
Generic Name acetaminophen, dextromethorphan hydrobromide, and phenylephrine hydrochloride
Labeler pharmadel llc
Dosage Form GRANULE, FOR SOLUTION
Routes
ORAL
Active Ingredients

acetaminophen 650 mg/1, dextromethorphan hydrobromide 20 mg/1, phenylephrine hydrochloride 10 mg/1

Manufacturer
Pharmadel LLC

Identifiers & Regulatory

Product NDC 55758-384
Product ID 55758-384_487431f0-067c-126f-e063-6394a90a0371
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2027-12-31
Marketing Start 2024-03-31

Pharmacologic Class

Classes
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]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 55758384
Hyphenated Format 55758-384

Supplemental Identifiers

RxCUI
1659967
UNII
362O9ITL9D 9D2RTI9KYH 04JA59TNSJ

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 sanatos severe cold and cough daytime (source: ndc)
Generic Name acetaminophen, dextromethorphan hydrobromide, and phenylephrine hydrochloride (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 650 mg/1
  • 20 mg/1
  • 10 mg/1
source: ndc
Packaging
  • 6 GRANULE, FOR SOLUTION in 1 CARTON (55758-384-06)
source: ndc

Packages (1)

Ingredients (3)

acetaminophen (650 mg/1) dextromethorphan hydrobromide (20 mg/1) phenylephrine hydrochloride (10 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "487431f0-067c-126f-e063-6394a90a0371", "openfda": {"unii": ["362O9ITL9D", "9D2RTI9KYH", "04JA59TNSJ"], "rxcui": ["1659967"], "spl_set_id": ["14484bf5-ff45-b859-e063-6394a90a9a0f"], "manufacturer_name": ["Pharmadel LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 GRANULE, FOR SOLUTION in 1 CARTON (55758-384-06)", "package_ndc": "55758-384-06", "marketing_start_date": "20240331"}], "brand_name": "SanaTos Severe Cold and Cough Daytime", "product_id": "55758-384_487431f0-067c-126f-e063-6394a90a0371", "dosage_form": "GRANULE, FOR SOLUTION", "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": "55758-384", "generic_name": "Acetaminophen, Dextromethorphan hydrobromide, and Phenylephrine hydrochloride", "labeler_name": "Pharmadel LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "SanaTos", "brand_name_suffix": "Severe Cold and Cough Daytime", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/1"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "20 mg/1"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240331", "listing_expiration_date": "20271231"}