DIABETIC TUSSIN DM MAXIMUM STRENGTH- dextromethorphan hydrobromide and guaifenesin liquid

Diabetic Tussin DM Maximum Strength by

Drug Labeling and Warnings

Diabetic Tussin DM Maximum Strength by is a Otc medication manufactured, distributed, or labeled by MEDTECH PRODUCTS INC, Akorn Operating Company LLC (dba Akorn). Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients (in each 10 mL)

Dextromethorphan hydrobromide 20 mg

Guaifenesin 400 mg

Purposes

Cough Suppressant

Expectorant

Uses

• temporarily relieves cough caused by the common cold or inhaled irritants.
• helps loosen phlegm (mucus) and thin bronchial secretions to rid bronchial passageways of bothersome mucus.

Warnings

Do not use

if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric or emotional conditions, or Parkinson's disease), or for two 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 cough that occurs with too much phlegm (mucus)
• a chronic cough that lasts or as occurs with smoking, asthma, chronic bronchitis, or emphysema

Stop use and ask a doctor if

• cough lasts more than 7 days, comes back, or occurs with fever, rash, or headache that lasts
•   These could be signs of a serious condition.

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

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

Directions

• take every 4 hours
• do not exceed 6 doses in 24 hours

• Adults:

  10 mL (2 teaspoons)

• Children under 12 years:

  ask a doctor

Other information

• store at room temperature 20-25ºC (68-77ºF)
• keep tightly closed

Inactive ingredients

Acesulfame K, artificial raspberry flavors, hypromellose, menthol, methylparaben, polyethylene glycol, potassium sorbate, purified water and sucralose. Citric acid may be used to adjust pH.

Questions or comments?

Call 1-800-579-8327, serious side effects associated with use of this product may be reported to this number.

Rev #515:00 04/19

Package Principal Display Panel

SUGAR & ALCOHOL FREE!

Specifically Formulated for Diabetics

Diabetic Tussin®

MAXIMUM STRENGTH

COUGH & CHEST CONGESTION

DM

Dextromethorphan HBr (Cough Suppressant)

Guaifenesin (Expectorant)

Relieves:

• Mucus
• Cough
• Sore throat
• Chest congestion

Improved Berry Flavor

4 FL OZ (118 mL)

INGREDIENTS AND APPEARANCE

DIABETIC TUSSIN DM MAXIMUM STRENGTH 
dextromethorphan hydrobromide and guaifenesin liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 61787-515
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS)	DEXTROMETHORPHAN HYDROBROMIDE	20 mg  in 10 mL
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ)	GUAIFENESIN	400 mg  in 10 mL

Inactive Ingredients
Ingredient Name	Strength
ACESULFAME POTASSIUM (UNII: 23OV73Q5G9)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
METHYLPARABEN (UNII: A2I8C7HI9T)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
RASPBERRY (UNII: 4N14V5R27W)
SUCRALOSE (UNII: 96K6UQ3ZD4)
WATER (UNII: 059QF0KO0R)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)

Product Characteristics
Color		Score
Shape		Size
Flavor	RASPBERRY (artificial raspberry flavor)	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 61787-515-04	1 in 1 BOX	02/01/2020
1		118 mL in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC: 61787-515-08	1 in 1 BOX	02/01/2020
2		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	02/01/2020

Labeler - Akorn Consumer Health (101196749)

Establishment
Name	Address	ID/FEI	Business Operations
Hi-Tech Pharmacal Co., Inc.		101196749	MANUFACTURE(61787-515)