CURATUSSIN- guaifenesin solution 
Wittman Pharma, Inc.

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CuraTUSSIN

Dosage & Admin

Directions:

■ do not take more than 6 doses in any 24-hour period.

AGEDOSE
Adults & Children 12 years and over2-4 teaspoonfuls every 4 hours
Children 6 years to under 12 years1-2 teaspoonfuls every 4 hours
Children 2 to under 6 years

1/2 - 1 teaspoonfuls every 4 hours

Children Under 2 yearsAsk a Doctor

Warnings

Warnings:

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 a 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.

If pregnant of 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.

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

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

medical help or contact a Poison Control Center right away.

Purpose: Expectorant

Active Ingredient (in each 5 mL tsp)

Guaifenesin 100 mg

CuraTUSSIN Label

CURATUSSIN 
guaifenesin solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83335-101
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN100 mg  in 5 mL
Inactive Ingredients
Ingredient NameStrength
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
POTASSIUM CITRATE (UNII: EE90ONI6FF)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
AMMONIUM GLYCYRRHIZATE (UNII: 3VRD35U26C)  
SORBITOL (UNII: 506T60A25R)  
WATER (UNII: 059QF0KO0R)  
Product Characteristics
Color    Score    
ShapeSize
FlavorGRAPEImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:83335-101-16473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/01/2024
2NDC:83335-101-08237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/01/2024
3NDC:83335-101-04118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/01/2024
Image of Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01201/01/2024
Labeler - Wittman Pharma, Inc. (830980947)
Establishment
NameAddressID/FEIBusiness Operations
Wittman Pharma, Inc.830980947analysis(83335-101) , manufacture(83335-101) , label(83335-101)

Revised: 4/2024
Document Id: 166317ec-4024-fd04-e063-6294a90a7b6a
Set id: 0fc8ab3f-23d8-ce01-e063-6394a90aab0f
Version: 4
Effective Time: 20240418
 
Wittman Pharma, Inc.