actidom dmx

Generic: dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride

Labeler: actipharma, llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name actidom dmx
Generic Name dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride
Labeler actipharma, llc
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

dextromethorphan hydrobromide 30 mg/5mL, guaifenesin 200 mg/5mL, phenylephrine hydrochloride 10 mg/5mL

Manufacturer
ACTIPHARMA, LLC

Identifiers & Regulatory

Product NDC 63102-110
Product ID 63102-110_07838a85-4ddc-470d-a344-001587f2d904
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2015-08-13

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 63102110
Hyphenated Format 63102-110

Supplemental Identifiers

RxCUI
1364914
UNII
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 actidom dmx (source: ndc)
Generic Name dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 30 mg/5mL
  • 200 mg/5mL
  • 10 mg/5mL
source: ndc
Packaging
  • 474 mL in 1 BOTTLE, PLASTIC (63102-110-16)
source: ndc

Packages (1)

63102-110-16 474 mL in 1 BOTTLE, PLASTIC (63102-110-16)

Ingredients (3)

dextromethorphan hydrobromide (30 mg/5mL) guaifenesin (200 mg/5mL) phenylephrine hydrochloride (10 mg/5mL)

Linked Drug Pages (1)

ACTIDOM DMX ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "07838a85-4ddc-470d-a344-001587f2d904", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1364914"], "spl_set_id": ["0166322e-7dbb-4658-a5c5-1d0525bb7655"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["ACTIPHARMA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "474 mL in 1 BOTTLE, PLASTIC (63102-110-16)", "package_ndc": "63102-110-16", "marketing_start_date": "20150813"}], "brand_name": "ACTIDOM DMX", "product_id": "63102-110_07838a85-4ddc-470d-a344-001587f2d904", "dosage_form": "SOLUTION", "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": "63102-110", "generic_name": "DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE", "labeler_name": "ACTIPHARMA, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ACTIDOM DMX", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "30 mg/5mL"}, {"name": "GUAIFENESIN", "strength": "200 mg/5mL"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "10 mg/5mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20150813", "listing_expiration_date": "20261231"}