Label: GILTUSS HBP COUGH AND CHEST CONGESTION- dextromethorphan hydrobromide, guaifenesin solution
- NDC Code(s): 65852-006-04
- Packager: Dextrum Laboratories Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated September 22, 2025
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- Official Label (Printer Friendly)
- Active ingredients
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Purposes and Uses
Purposes
Cough supresant
Expectorant
Uses
Temporary relieves, cough due to minor throat and bronchial irritation as may occur with the common cold or inhaled irritants , the intensity of coughing, the impulse to cough to help you get to sleep, help loosen phlegm ( mucus) and thin bronchial secretions to make cough more productive and drain bronchial tubes

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Warnings
Warnings
Do not use
If you are taking a prescription monoamine oxidase inhibitor (MAOI) ( certains drugs for depression, psychiatric, or emotional conditions, or Parkinson's disease), or for 2 weeks after stopping the MAOI drug. If you dont know is your prescription drug contains and MAOI, ask a doctor or pharmacist before taking this product.

- Ask a doctor
- Stop use and ask a doctor
- If pregnant
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Directions
Directions
Do not exceed recommended dosage
Do not take more than 6 doses in any 24 hours period
Keep dosing cup with product
ml= mililiters
Adults and children 12 years & over 10 ml every 4 hours
children 6 to under 12 years of age 5 ml every 4 hours
children 4 to under 6 years of age 2.5 ml every 4 hours
children under 4 years of age Consult a doctor

- Other information
- Inactive Ingredients
- Questions or comments
- keep out of seach children
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INDICATIONS & USAGE
Indication and usage
Do not exceed recommended dosage
Do not take more than 6 doses in any 24 hours period
Keep dosing cup with product
ml= mililiters
Adults and children 12 years & over 10 ml every 4 hours
children 6 to under 12 years of age 5 ml every 4 hours
children 4 to under 6 years of age 2.5 ml every 4 hours
children under 4 years of age Consult a doctor

- Principal panel
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INGREDIENTS AND APPEARANCE
GILTUSS HBP COUGH AND CHEST CONGESTION
dextromethorphan hydrobromide, guaifenesin solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:65852-006 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN 200 mg in 10 mL DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE 20 mg in 10 mL Inactive Ingredients Ingredient Name Strength CITRIC ACID (UNII: 2968PHW8QP) RASPBERRY (UNII: 4N14V5R27W) PROPYLPARABEN (UNII: Z8IX2SC1OH) METHYLPARABEN (UNII: A2I8C7HI9T) WATER (UNII: 059QF0KO0R) SUCRALOSE (UNII: 96K6UQ3ZD4) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) Product Characteristics Color Score Shape Size Flavor RASPBERRY Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:65852-006-04 1 in 1 CARTON 11/13/2018 1 118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M012 11/13/2018 Labeler - Dextrum Laboratories Inc. (007392322)


Maximum strength