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Scot-Tussin DM SF Maximum Strength Cough Cold

Dosage form: liquid
Ingredients: DEXTROMETHORPHAN HYDROBROMIDE 15mg in 5mL, CHLORPHENIRAMINE MALEATE 2mg in 5mL
Labeler: SCOT-TUSSIN Pharmacal Co., Inc.
NDC Code: 0372-0036

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.

Scot-Tussin DM SF Maximum Strength Cough Cold

Active Ingredients

(in each 5 mL. tsp. teaspoon)

*Chlorpheniramine Maleate USP 2mg

Dextromethorphan HBr. USP 15mg 

Purpose

Antihistamine

Cough Suppressant

Uses
  • Temporarily relieves cough due to minor throat and bronchial irritation as may occur with a cold. Quiets and calms a dry cough.
  • Temporarily relieves runny nose and sneezing, itching of the nose and throat, and itchy watery eyes due to upper respiratory symptoms.

Warnings

DO NOT USE THIS PRODUCT TO SEDATE CHILDREN

Do not use 
  • more than the recommended dosage.
  • if you are 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 pharmacists before taking this product.

Ask a doctor before use is you have
  • Persistent or a chronic cough such as occurs with smoking, asthma, chronic bronchitis or emphysema, or if cough is accompanied by excessive phlegm (mucus).
  • Difficulty in urination due to enlargement of the prostate gland.
  • Glaucoma.
  • Thyroid disease.

When using this product
  • May cause drowsiness. Alcohol, sedatives and tranquilizers may increase the drowsiness effect. Avoid alcoholic beverages while taking this product. If you are taking sedatives or tranquilizers, consult your doctor before taking this medicine. Use caution when driving a motor vehicle or operating machinery.

Stop use and ask a doctor if
  • Chough lasts more than seven days, returns or is accompanied by fever, rash or persistent headache. These could be signs of a serious condition.

If pregnant or breast-feeding,

Do Not Use.

Keep out of reach of children.

In case of overdose get medical help or contact a Poison Control Center right away.

Directions:
  • Follow Dosage Chart.
  • Do not take more than 4 doses in any 24 hour period.
  • This product is not intended for use in children under 12 years of age.
agedose
Adults and children
over 12 years old
2 teaspoons
(2 tsp. 10 ml)
every 6 hours
Children Under
12 years old
DO NOT USE

Other Information
  • Store at 20º – 25º C (68º – 77º F).
  • Do not refrigerate.
  • Dosage cup provided.

Inactive Ingredients

Ammonium Glycrrhizate, Citric Acid, Clear Cherry-Strawberry Flavor, Glycerin, Hydroxyethylcellulose, Menthol, Methyl Paraben, Potassium Benzoate, Propyl Paraben, Propylene Glycol, Purified Water.

PRINCIPAL DISPLAY PANEL

NDC 0372-0036-04

SCOT-TUSSIN

DM

Maximum Strength
COUGH SUPPRESSANT & COLD RELIEF

4 FL OZ (118 ml)

SCOT-TUSSIN  DM SF MAXIMUM STRENGTH COUGH COLD
dextromethorphan hydrobromide chlorpheniramine maleate liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0372-0036
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DEXTROMETHORPHAN HYDROBROMIDE (DEXTROMETHORPHAN) DEXTROMETHORPHAN HYDROBROMIDE15 mg  in 5 mL
CHLORPHENIRAMINE MALEATE (CHLORPHENIRAMINE) CHLORPHENIRAMINE MALEATE2 mg  in 5 mL
Inactive Ingredients
Ingredient NameStrength
AMMONIUM GLYCYRRHIZATE 
CITRIC ACID MONOHYDRATE 
GLYCERIN 
HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%) 
MENTHOL 
METHYLPARABEN 
POTASSIUM BENZOATE 
PROPYLENE GLYCOL 
PROPYLPARABEN 
WATER 
Product Characteristics
Color    Score    
ShapeSize
FlavorSTRAWBERRY, CHERRYImprint Code
Contains    
Packaging
#Item CodePackage Description
1NDC:0372-0036-04118 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart34109/28/1983
Labeler - SCOT-TUSSIN Pharmacal Co., Inc. (001203918)

Revised: 01/2013
 
SCOT-TUSSIN Pharmacal Co., Inc.

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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