multi symptom severe cold

Generic: acetaminophen, dextromethorphan hbr, phenylephrine hcl

Labeler: raritan pharmaceuticals inc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name multi symptom severe cold
Generic Name acetaminophen, dextromethorphan hbr, phenylephrine hcl
Labeler raritan pharmaceuticals inc
Dosage Form POWDER, FOR SOLUTION
Routes
ORAL
Active Ingredients

acetaminophen 500 mg/1, dextromethorphan hydrobromide 20 mg/1, phenylephrine hydrochloride 10 mg/1

Manufacturer
RARITAN PHARMACEUTICALS INC

Identifiers & Regulatory

Product NDC 68163-547
Product ID 68163-547_3fc363f2-3364-b03f-e063-6294a90af150
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2019-04-10

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 68163547
Hyphenated Format 68163-547

Supplemental Identifiers

RxCUI
1189316
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 multi symptom severe cold (source: ndc)
Generic Name acetaminophen, dextromethorphan hbr, phenylephrine hcl (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
  • 20 mg/1
  • 10 mg/1
source: ndc
Packaging
  • 6 POWDER, FOR SOLUTION in 1 CARTON (68163-547-06)
source: ndc

Packages (1)

Ingredients (3)

acetaminophen (500 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": "3fc363f2-3364-b03f-e063-6294a90af150", "openfda": {"unii": ["362O9ITL9D", "9D2RTI9KYH", "04JA59TNSJ"], "rxcui": ["1189316"], "spl_set_id": ["d9606c9a-31b1-4121-9870-809a05f5b68a"], "manufacturer_name": ["RARITAN PHARMACEUTICALS INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 POWDER, FOR SOLUTION in 1 CARTON (68163-547-06)", "package_ndc": "68163-547-06", "marketing_start_date": "20190410"}], "brand_name": "Multi Symptom Severe Cold", "product_id": "68163-547_3fc363f2-3364-b03f-e063-6294a90af150", "dosage_form": "POWDER, 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": "68163-547", "generic_name": "ACETAMINOPHEN, DEXTROMETHORPHAN HBr, PHENYLEPHRINE HCl", "labeler_name": "RARITAN PHARMACEUTICALS INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Multi Symptom Severe Cold", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 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": "20190410", "listing_expiration_date": "20261231"}