SCOT-TUSSIN DM SF MAXIMUM STRENGTH COUGH COLD- dextromethorphan hydrobromide chlorpheniramine maleate liquid

Scot-Tussin by

Drug Labeling and Warnings

Scot-Tussin by is a Otc medication manufactured, distributed, or labeled by SCOT-TUSSIN Pharmacal Co., Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

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.

• age: dose
• 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)

INGREDIENTS AND APPEARANCE

SCOT-TUSSIN  DM SF MAXIMUM STRENGTH COUGH COLD
dextromethorphan hydrobromide chlorpheniramine maleate liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0372-0036
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS)	DEXTROMETHORPHAN HYDROBROMIDE	15 mg  in 5 mL
CHLORPHENIRAMINE MALEATE (UNII: V1Q0O9OJ9Z) (CHLORPHENIRAMINE - UNII:3U6IO1965U)	CHLORPHENIRAMINE MALEATE	2 mg  in 5 mL

Inactive Ingredients
Ingredient Name	Strength
AMMONIUM GLYCYRRHIZATE (UNII: 3VRD35U26C)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
GLYCERIN (UNII: PDC6A3C0OX)
HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%) (UNII: S38J6RZN16)
MENTHOL (UNII: L7T10EIP3A)
METHYLPARABEN (UNII: A2I8C7HI9T)
POTASSIUM BENZOATE (UNII: 763YQN2K7K)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
WATER (UNII: 059QF0KO0R)

Product Characteristics
Color		Score
Shape		Size
Flavor	STRAWBERRY, CHERRY	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0372-0036-04	118 mL in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part341	09/28/1983

Labeler - SCOT-TUSSIN Pharmacal Co., Inc. (001203918)