SCOT-TUSSIN DIABETES COUGH FORMULA WITH DM- dextromethorphan hydrobromide liquid
SOCIETAL CDMO SAN DIEGO, LLC

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 Diabetes Cough Suppressant Formula With DM

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)

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
DR

SCOT-TUSSIN DIABETES COUGH FORMULA WITH DM
dextromethorphan hydrobromide liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:15187-043
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS)	DEXTROMETHORPHAN HYDROBROMIDE	10 mg in 5 mL

Ingredient Name	Strength
Inactive Ingredients
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

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:15187-043-04	1 in 1 CARTON	01/01/2016	05/31/2023
1		118 mL in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC:15187-043-08	1 in 1 CARTON	08/01/2018	05/31/2023
2		237 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part341	01/01/2016	05/31/2023

Labeler - SOCIETAL CDMO SAN DIEGO, LLC (079682716)

Revised: 5/2023

Document Id: fc10e25f-edc4-4dd1-e053-6294a90a53f6

Set id: fb5282f3-e7b5-4b3a-9919-6ad316508e05

Version: 8

Effective Time: 20230519

SOCIETAL CDMO SAN DIEGO, LLC