SCOT-TUSSIN DIABETES COUGH FORMULA WITH DM- dextromethorphan hydrobromide liquid

Scot-Tussin Diabetes Cough Formula with DM by

Drug Labeling and Warnings

Scot-Tussin Diabetes Cough Formula with DM by is a Otc medication manufactured, distributed, or labeled by SOCIETAL CDMO SAN DIEGO, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient (in each 5 mL. tsp. teaspoon)

 Dextromethorphan HBr. USP 10 mg

Purpose

Cough Suppressant

Uses

• temporarily quiets and calms a dry cough due to minor throat and bronchial irritation.

Warnings

Do not use:

• more than the recommended dosage. If drowsiness occurs, do not drive or operate machinery.
  
• 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 pharmacist before taking this product.

Ask a doctor before use if you have

• a chronic cough such as occurs with smoking, asthma, chronic bronchitis or emphysema.
  
• difficulty in urination due to enlargement of the prostate gland.
  
• glaucoma.
  
• thyroid disease.
  
• a cough that occurs with too much phlegm (mucus).

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 accidental overdose get medical help or contact a Poison Control Center right away.

Directions

• follow Dosage Chart.
  
• do not take more than 6 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 4 hours
• Children under 12 years old: DO NOT USE

Other information

• store at 20° - 25° C (68° - 77° F).
  
• do not refrigerate.
  
• dosage cup provided.

Inactive ingredients

Ammonium glycyrrhizate, citric acid, clear cherry-strawberry flavor, glycerin, hydroxyethylcellulose, menthol, methyl-paraben, potassium benzoate, propyl-paraben, propylene glycol, purified water.

Distributed by:
IriSys, LLC
San Diego, CA 92121 U.S.A.
Questions? 1-800-638-7268
www.scot-tussin.com
®TM Reg. US Patent Office No. 657, 674

PRINCIPAL DISPLAY PANEL

SUGAR-FREE
ADULT
NDC: 15187-043-04
For Diabetics since 1956
SCOT-TUSSIN ®
DIABETES
COUGH SUPPLESSANT
Formula with DM
DEXTROMETHORPHAN HBr (Cough Suppressant)

FAST RELIEF OFF
DRY HACKING COUGH

• FIRST SUGAR & ALCOHOL-FREE
  
• HIGH BLOOD PRESSURE SAFE
  
• LACTOSE & GLUTEN-FREE
  
• SODIUM-FREE
  
• DYE-FREE

LIQUID

4 FL OZ (118 ml)

INGREDIENTS AND APPEARANCE

SCOT-TUSSIN DIABETES COUGH FORMULA WITH DM 
dextromethorphan hydrobromide liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 15187-045
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS)	DEXTROMETHORPHAN HYDROBROMIDE	10 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, UNSPECIFIED FORM (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	CHERRY (clear cherry-strawberry flavor) , STRAWBERRY (clear cherry-strawberry flavor)	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 15187-045-08	1 in 1 CARTON	08/01/2018
1		237 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part341	01/01/2016

Labeler - IriSys, LLC (079682716)