SCOT-TUSSIN EXPECTORANT SF COUGH- guaifenesin liquid 
SCOT-TUSSIN Pharmacal Co., 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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Scot-Tussin Expectorant SF Cough

Active Ingredient: 

(in each 5 mL. tsp. teaspoon)

Guaifenesin 100mg

Purpose

Expectorant

Uses

Warnings

When using this product

  • Don’t take more than the recommended dosage.

Ask a doctor before use if you have

  • a Cough that occurs with too much phlegm (mucus).
  • a Chronic cough such as occurs with smoking, asthma, chronic bronchitis or emphysema.

Stop use and ask a doctor if

  • Cough 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:

age dose
Adults and children
over 12 years old
2 teaspoons
(2 tsp. 10 ml)
every 4 hours
Children Under
12 years old
DO NOT USE

Other Information

Inactive Ingredients

Aspartame* (see warning) Benzoic Acid, Citric Acid, Clear Grape Flavor, Glycerin, Hydroxypropylmethylcellulose, Menthol, Methyl Paraben, Propyl Paraben, Propylene Glycol, Purified Water.

PRINCIPAL DISPLAY PANEL

NDC 0372-0006-04

SCOT-TUSSIN

EXPECTORANT

COUGH

4 FL OZ (118 ml)

Principal Display Panel

SCOT-TUSSIN EXPECTORANT SF COUGH 
guaifenesin liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:0372-0006
Route of Administration ORAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN 100 mg  in 5 mL
Inactive Ingredients
Ingredient Name Strength
ASPARTAME (UNII: Z0H242BBR1)  
BENZOIC ACID (UNII: 8SKN0B0MIM)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
GLYCERIN (UNII: PDC6A3C0OX)  
HYPROMELLOSES (UNII: 3NXW29V3WO)  
MENTHOL (UNII: L7T10EIP3A)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
Product Characteristics
Color      Score     
Shape Size
Flavor GRAPE Imprint Code
Contains     
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:0372-0006-04 118 mL in 1 BOTTLE
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC MONOGRAPH FINAL part341 07/01/1974
Labeler - SCOT-TUSSIN Pharmacal Co., Inc. (001203918)

Revised: 1/2013
Document Id: a02a5ca8-8c0d-4be5-92b1-5271d555f252
Set id: 2cd6ab31-1fae-4737-b6af-50586323b751
Version: 4
Effective Time: 20130129
 
SCOT-TUSSIN Pharmacal Co., Inc.