DIABETIC TUSSIN DM MAXIMUM STRENGTH- dextromethorphan hydrobromide and guaifenesin liquid 
MEDTECH PRODUCTS 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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DiabeticTussin DM Max Strength 61787-515

Drug Facts

Active ingredients (in each 10 mL)

Dextromethorphan hydrobromide 20 mg

Guaifenesin 400 mg

Purposes

Cough Suppressant

Expectorant

Uses

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

Adults10 mL (2 teaspoons)
Children under 12 yearsask a doctor

Other information

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.

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:

Improved Berry Flavor

4 FL OZ (118 mL)

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)

DIABETIC TUSSIN DM MAXIMUM STRENGTH 
dextromethorphan hydrobromide and guaifenesin liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:61787-515
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE20 mg  in 10 mL
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN400 mg  in 10 mL
Inactive Ingredients
Ingredient NameStrength
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    
ShapeSize
FlavorRASPBERRY (artificial raspberry flavor) Imprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:61787-515-041 in 1 BOX02/01/2020
1118 mL in 1 BOTTLE; Type 0: Not a Combination Product
2NDC:61787-515-081 in 1 BOX02/01/2020
2237 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34102/01/2020
Labeler - MEDTECH PRODUCTS INC (114707784)
Establishment
NameAddressID/FEIBusiness Operations
Akorn Operating Company LLC (dba Akorn)117696873manufacture(61787-515)

Revised: 3/2022
Document Id: e4cd7371-f717-4109-bba6-c26dbaecedc7
Set id: a10a3b33-7503-4334-8ed7-2bb881df4327
Version: 3
Effective Time: 20220303
 
MEDTECH PRODUCTS INC