DOUBLE TUSSIN INTENSE COUGH RELIEVER DM- dextromethorphan hydrobromide / guaifenesin liquid
Reese Pharmaceutical Co
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.
----------
Active ingredient per 5ml teaspoon
Dextromethorphan Hydrobromide 20mg Cough Suppressant
Guaifenesin 300mg Expectorant
Uses. temporarily relieves cough due to minor throat and bronchial irritation
as may occur with a common cold • helps loosen phlegm (mucus) and thin
bronchial secretions to rid the bronchial passageways of bothersome mucus
• helps make coughs more productive
Do not use if you are now taking a prescription monoamine oxidase (inhiMor~MAIO)
Certain drugs for depression, psychiatric or emotional conditioners or Parkinson's disease
or for 2 weeks after stopping MAIO drug, If you do not know if your prescription drug contains
an MAIO, ask your doctor or pharmacist before using this product
Ask doctor before use if you have
persistent or chronic cough, such as occurs with smoking, asthma, bronchitis or emphysma
cough is accompanied by excessive phlegm (mucous)
Stop use and ask doctor if
Symptoms are accompanied by fever, rash or persistent headache
cough persists for more than 1 week or tends to recur
A persistent cough may be a sign of a serious condition
Keep out of reach of children, In case of overdose, get medical help or contact a Poison Center immediately
Directions
• Adults and children 12 years of age and over:
take 1 tablet every 4 hours as needed
• Children 6 to 10 under 12 years of age: take 1/2 tablet every 4 hours as needed
• Children under 6 years of age: consult a doctor
Do not exceed 6 doses in a 24 hour period or as directed by a doctor
Other information store at 15'- 30' C (59'- 86'F)
DOUBLE TUSSIN INTENSE COUGH RELIEVER
DM
dextromethorphan hydrobromide / guaifenesin liquid |
|||||||||||||||||||||||||
|
|||||||||||||||||||||||||
|
|||||||||||||||||||||||||
|
|||||||||||||||||||||||||
|
|||||||||||||||||||||||||
|
|||||||||||||||||||||||||
|
Labeler - Reese Pharmaceutical Co (004172052) |
Registrant - Reese Pharmaceutical Co (004172052) |
Establishment | |||
Name | Address | ID/FEI | Business Operations |
---|---|---|---|
Reese Pharmaceutical Co | 004172052 | relabel, repack |