Label: GILTUSS HONEY COUGH AND CHEST CONGESTION- dextromethorphan hbr, guaifenesin liquid
- NDC Code(s): 65852-005-04
- Packager: Dextrum Laboratories, Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated September 29, 2025
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Indication and user panel
Indication and user section:
Do not take more than 6 doses in any 24-hours perio. use enclosed dosing cup
- Keep dosage cup for use whit this product
- ml= milliliters
Adults and childrens 12 years and over 10ml every 4 hours
Children 6 to 12 years of age 5 ml every 4 hours
Children 4 to under 6 years of age 2.5ml every 4 hous
Children under 4 yeras of age Consult a doctor
- Active ingredient
- PURPOSE
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Warnings
Warnings
Do not use if you are now taking a prescription monoamine oxidase inhibidor (MAOI) (Certain drugs for depression, psychiatric or emotional conditions, or Parkinson's desease), or for two weeks after stopping the MAOI drug. If you do not know if you prescription drug constains an MAOI, ask a doctor or pharmacist before taking this product.
- Keep out of the reach of the children
- Pregnant or breast feedings
- Dosage and Administration
- INACTIVE INGREDIENT
- Question section
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Warnings
Warnings:
Do not use if you are now taking a prescription monoamine oxidase inhibidor (MAOI) (Certain drugs for depression, psychiatric or emotional conditions, or Parkinson's desease), or for two weeks after stopping the MAOI drug. If you do not know if you prescription drug constains an MAOI, ask a doctor or pharmacist before taking this product.
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principal display panel
Maximum strength. Maxima Concentracion
Alcohol Free
Dye free
Non-Drowsy
True source
Certified Honey
Giltuss Honey Cough % Chest Congestion
Tos y congestion de Pecho
cough and cold, chest Tos y catarro,
Congestion, liquifies Congestion de Pecho,
and loosens phlegm and mucus Licua y suelt LA FLEMA Y EL MOCO
Honey Lemon flavor. Sabor a Miel y limon 4FL OZ (118ml)
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INGREDIENTS AND APPEARANCE
GILTUSS HONEY COUGH AND CHEST CONGESTION
dextromethorphan hbr, guaifenesin liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:65852-005 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 METHYLPARABEN (UNII: A2I8C7HI9T) WATER (UNII: 059QF0KO0R) PROPYLPARABEN (UNII: Z8IX2SC1OH) CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) SUCRALOSE (UNII: 96K6UQ3ZD4) GLYCERIN (UNII: PDC6A3C0OX) HONEY (UNII: Y9H1V576FH) CITRIC ACID (UNII: 2968PHW8QP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:65852-005-04 1 in 1 CARTON 06/22/2020 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 06/22/2020 Labeler - Dextrum Laboratories, Inc (007392322)
