DIABETIC MAXIMUM STRENGTH SILTUSSIN DM DAS-NA
-
guaifenesin and
dextromethorphan hydrobromide liquid
Silarx Pharmaceuticals, Inc
Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
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Active Ingredient: Guaifenesin 200 mg (in each 5 mL)
Active Ingredient: Dextromethorphan Hydrobromide 10 mg (in each 5 mL)
Uses
■ temporarily relieves cough due to minor throat and bronchial irritation
■ helps loosen phlegm (mucus)
■ thin bronchial secretions to make coughs more productive
Do not use if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric or emotional conditions, or Parkinson’s disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product.
Ask a doctor before use if you have
■ persistent cough or chronic cough such as occurs with smoking, asthma, chronic bronchitis, emphysema
■ cough accompanied by excessive phlegm (mucus)
take every 4 hours, or as directed by a doctor, not more than 6 doses in 24 hours
Adult and children 12 years and over | 2 teaspoonfuls (10 mL) |
Children under 12 years | DO NOT USE |
Acesulfame-K, aspartame, benzoic acid, hydroxypropyl methyl cellulose, methylparaben, propylene glycol, strawberry flavor, and water. May contain citric acid.
■ store at room temperature 20°-25°C (68°-77°F)
■ Phenylketonurics: contains phenylalanine 3 mg per teaspoonful (5 mL)
888-974-5279
*This product is not manufactured or distributed by Wyeth Consumer Healthcare, distributor of Robitussin®-DM.
Manufactured by:
Silarx Pharmaceuticals, Inc
19 West Street
Spring Valley, NY 10977
USA
DIABETIC MAXIMUM STRENGTH SILTUSSIN DM DAS-NA
guaifenesin and dextromethorphan hydrobromide liquid |
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Marketing Information | |||
Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
OTC monograph final | part341 | 11/05/2005 |
Labeler - Silarx Pharmaceuticals, Inc (161630033) |
Revised: 06/2011 Silarx Pharmaceuticals, Inc