CURATUSSIN DM- dextromethorphan hbr/guaifenesin liquid 
Wittman Pharma, Inc.

----------

CuraTUSSIN DM

Directions:
■ follow dosage below or use as directed by a physician
■ do not take more than 6 doses in any 24-hour period

Dosage Table

Warnings: Do not use if you are now taking a prescription monoamine oxidase inhibitor (MADI)
(certain drugs for depression, psychiatric or emotional conditions, or Parkinson's disease),or for 2
weeks after stopping the MADI drug.If you do not know if your
prescription drug contains an MAOI; ask a doctor or pharmacist before taking this product.t
Ask a doctor before use if you have
■ cough that occurs with too much phlegm (mucus)
■ cough that lasts or is chronic, such as occurs with smoking, asthma,
chronic bronchitis, or emphysema
Stop use and ask doctor if


■cough lasts more than 7 days., comes back, or is accompanied by fever, rash, or persistent headache. These could be signs of a serious condition.
■you are hypersensitive to any of the ingredients.

If pregnant or breastfeeding, 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.

Inactive Ingredients: Citric Acid, Flavor, Methylparaben, Monoammonium Glycyrrhizinate, Potassium Citrate, Propylene Glycol, Propylparaben, Purified Water, Sorbitol, Sucralose

Uses:

■ helps loosen phlegm(mucus) and thin bronchial secretions to make coughs more productive

■ temporarily relieves cough due to minor throat and bronchial irritation as may occur with a cold

Keep out of reach of children. In case of overdose, get

medical help or contact a Poison Control Center right away.

Purpose:

Cough Suppressant and Expectorant

Active Ingredient (in each 5 mL tsp)

Dextromethorphan HBr 10mg

Guaifenesin 100mg

CuraTUSSIN DM Label

CURATUSSIN DM 
dextromethorphan hbr/guaifenesin liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83335-102
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN100 mg  in 5 mL
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE10 mg  in 5 mL
Inactive Ingredients
Ingredient NameStrength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
AMMONIUM GLYCYRRHIZATE (UNII: 3VRD35U26C)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
POTASSIUM CITRATE (UNII: EE90ONI6FF)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
WATER (UNII: 059QF0KO0R)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
SORBITOL (UNII: 506T60A25R)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
Product Characteristics
Color    Score    
ShapeSize
FlavorGRAPEImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:83335-102-16473 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product03/01/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01203/01/2024
Labeler - Wittman Pharma, Inc. (830980947)
Establishment
NameAddressID/FEIBusiness Operations
Wittman Pharma, Inc.830980947analysis(83335-102) , manufacture(83335-102) , label(83335-102)

Revised: 4/2024
 
Wittman Pharma, Inc.