GUAIFENESIN STRAWBERRY-BANANA FLAVOR- guaifenesin liquid 
Innovida Pharmaeutique Corporation

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Active Ingredient 

Guaifenesin,USP 100 mg (in each 5ml tsp)

Purpose

Expectorant

Uses

Warnings

Do not take this product for persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysema, or where cough is accompanied by excessive phlegm (mucus) unless directed by a doctor.

Stop use and ask a doctor if■ cough persists for more than a week, tends to recur, or is accompanied by a fever, rash or persistent headache, consult a doctor. A persistent cough may be a sign of a serious condition.

If pregnant or breast-feeding, ask a health professional before use. Keep out of the reach of children. In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

 age dose

 Adults and Children 12 years of age and over:

Children under 12 years of age:

 Take 2-4 teaspoonful (5mL) every 4 hours

Consult a physician

Other Information

Inactive Ingredients

Citric acid, FD&C yellow #5, glycerin, methylparaben, potassium sorbate, propylene glycol, propylparaben, purified water, sodium citrate, strawberry-banana flavor, sucralose.

Questions or Comments? 1-888-462-4166

Product label

image description

GUAIFENESIN STRAWBERRY-BANANA FLAVOR 
guaifenesin liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71800-059
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
CITRIC ACID (UNII: 2968PHW8QP)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
GLYCERIN (UNII: PDC6A3C0OX)  
MENTHOL (UNII: L7T10EIP3A)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
WATER (UNII: 059QF0KO0R)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
STRAWBERRY (UNII: 4J2TY8Y81V)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71800-059-19119 mL in 1 TUBE; Type 0: Not a Combination Product06/16/2025
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01206/16/2025
Labeler - Innovida Pharmaeutique Corporation (080892908)

Revised: 6/2025
Document Id: 37de006a-e717-a4e5-e063-6394a90abd8b
Set id: 1006906e-d6d7-4f49-92bf-3cb2d2cdbb16
Version: 1
Effective Time: 20250618
 
Innovida Pharmaeutique Corporation