sanatos multi symptom

Generic: acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hci

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

Drug Facts

Product Profile

Brand Name sanatos multi symptom
Generic Name acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hci
Labeler pharmadel llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

acetaminophen 325 mg/1, dextromethorphan hydrobromide 15 mg/1, guaifenesin 200 mg/1, phenylephrine hydrochloride 5 mg/1

Manufacturer
Pharmadel LLC

Identifiers & Regulatory

Product NDC 55758-361
Product ID 55758-361_3cf6f937-1511-460f-e063-6294a90abde7
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2020-08-01

Pharmacologic Class

Established (EPC)
expectorant [epc]
Physiologic Effect
decreased respiratory secretion viscosity [pe] increased respiratory secretions [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 55758361
Hyphenated Format 55758-361

Supplemental Identifiers

RxCUI
1367204
UNII
362O9ITL9D 9D2RTI9KYH 495W7451VQ 04JA59TNSJ
NUI
N0000193956 N0000008867 N0000009560

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 multi symptom (source: ndc)
Generic Name acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hci (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 325 mg/1
  • 15 mg/1
  • 200 mg/1
  • 5 mg/1
source: ndc
Packaging
  • 2 TABLET in 1 PACKET (55758-361-02)
  • 50 PACKET in 1 CARTON (55758-361-99) / 2 TABLET in 1 PACKET (55758-361-02)
source: ndc

Packages (2)

55758-361-02 2 TABLET in 1 PACKET (55758-361-02) 55758-361-99 50 PACKET in 1 CARTON (55758-361-99) / 2 TABLET in 1 PACKET (55758-361-02)

Ingredients (4)

acetaminophen (325 mg/1) dextromethorphan hydrobromide (15 mg/1) guaifenesin (200 mg/1) phenylephrine hydrochloride (5 mg/1)

Linked Drug Pages (1)

SanaTos Multi Symptom ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3cf6f937-1511-460f-e063-6294a90abde7", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["362O9ITL9D", "9D2RTI9KYH", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1367204"], "spl_set_id": ["df260190-89e7-b338-e053-2995a90a32cb"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Pharmadel LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 TABLET in 1 PACKET (55758-361-02)", "package_ndc": "55758-361-02", "marketing_start_date": "20200801"}, {"sample": false, "description": "50 PACKET in 1 CARTON (55758-361-99)  / 2 TABLET in 1 PACKET (55758-361-02)", "package_ndc": "55758-361-99", "marketing_start_date": "20200801"}], "brand_name": "SanaTos Multi Symptom", "product_id": "55758-361_3cf6f937-1511-460f-e063-6294a90abde7", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]", "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": "55758-361", "generic_name": "Acetaminophen, dextromethorphan HBr, guaifenesin, phenylephrine HCI", "labeler_name": "Pharmadel LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "SanaTos Multi Symptom", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "15 mg/1"}, {"name": "GUAIFENESIN", "strength": "200 mg/1"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200801", "listing_expiration_date": "20261231"}