Actidom Dmx Solution
FDA Label NDC 63102-110
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Actipharma, Llc for the product Actidom Dmx (NDC 63102-110). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding drug facts, active ingredients (in each 5 ml tsp), purpose, otc - keep out of reach of children, other, packaging, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredients (In Each 5 Ml Tsp)
Dextromethorphan HBr, 30 mg
Guaifenesin, 200 mg
Phenylephrine HCl, 10 mg
Purpose
Cough Suppressant
Expectorant
Nasal Decongestant
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. In case of accidental overdose, get medical help or contact a Poison Control Center right away.
Other
Manufactured in the USA for ActiPharma, Inc. Dorado, PR 00646. Tel: (787)608-0882
* Dometuss-DMX® is a registered trademark of Domel Laboratories. This product is not manufactured, distributed or marketed by Domel Laboratories.
Contains the same active ingredients as Dometuss®-DMX*
COUGH SUPPRESSANT
EXPECTORANT
NASAL DECONGESTANT
SUGAR FREE
ALCOHOL FREE
Grape Flavor
* Please review the disclaimer below.
