DIABETIC TUSSIN EXPECTORANT- 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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Diabetic Tussin Expectorant 61787 514

DIABETIC TUSSIN EXPECTORANT- guaifenesin liquid 
Medtech Products Inc., a Prestige Consumer Healthcare company

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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Drug Facts

Active ingredient (in each 10 mL)

Guaifenesin 200 mg

Purpose

Expectorant

Uses

Warnings

Ask a doctor before use if you have:

  • a cough that occurs with too much phlegm (mucus)
  • a persistent or chronic cough such 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 - 20 mL (2 - 4 teaspoons)
Children under 12 yearsask a doctor

Other information

Inactive ingredients

Acesulfame K, artificial cherry flavor, artificial vanilla flavor, aspartame, hypromellose, menthol, methylparaben, potassium sorbate, purified water. 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 #0514:00 04/19

Principal Display Panel

SUGAR & ALCOHOL FREE!

Specifically Formulated for Diabetics

Diabetic Tussin®

CHEST CONGESTION

Guaifenesin (Expectorant)

Thins & Loosens Mucus

4 FL OZ (118 mL)

Diagram

Description automatically generated

DIABETIC TUSSIN EXPECTORANT 
guaifenesin liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:61787-514
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN200 mg  in 10 mL
Inactive Ingredients
Ingredient NameStrength
ACESULFAME POTASSIUM (UNII: 23OV73Q5G9)  
ASPARTAME (UNII: Z0H242BBR1)  
CHERRY (UNII: BUC5I9595W)  
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
VANILLA (UNII: Q74T35078H)  
WATER (UNII: 059QF0KO0R)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
Product Characteristics
Color    Score    
ShapeSize
FlavorCHERRY (artificial cherry flavor) , VANILLA (artificial vanilla flavor) Imprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:61787-514-041 in 1 BOX02/01/2020
1118 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(61787-514)

Revised: 3/2022
Document Id: 27e059a5-ece3-4fa7-8f12-59ae0c21bdd4
Set id: d65f7ad8-8dbc-4a29-8b42-0c6d5d7f4ffc
Version: 3
Effective Time: 20220307
 
MEDTECH PRODUCTS INC