Label: WALGREEN ADULT COUGH PLUS CHEST CONGESTION DM- dextromethorphan hydrobromide and guaifenesin solution
- NDC Code(s): 0363-7440-08
- Packager: WALGREEN COMPANY
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 12, 2024
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- Official Label (Printer Friendly)
- Active ingredients (in each 20 ml)
- INDICATIONS & USAGE
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WARNINGS
Warnings
Do not use if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric, or emotional conditions, or Parkinson's disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product.
Ask a doctor before use if you have
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- cough that occurs with too much phlegm (mucus)
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- cough that lasts or is chronic such as occurs with smoking, asthma, chronic bronchitis, or emphysema
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DOSAGE & ADMINISTRATION
Directions
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- do not take more than 6 doses in any 24-hour period
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- measure only with dosing cup provided
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- keep dosing cup with product
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- ml = milliliter
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- this adult product is not intended for use in children under 12 years of age
age
dose
adults and children 12 years and over
20 ml every 4 hours
children under 12 years
do not use
- STORAGE AND HANDLING
- INACTIVE INGREDIENT
- QUESTIONS
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PRINCIPAL DISPLAY PANEL
Compare to the active ingredients in Dye-Free Sugar-Free Adult Robitussin Cough + Chest Congestion DM*
NDC 0363-7440-08
DYE-FREEAdult
Cough+Chest
Congestion DMDextromethorphan HBr (Cough Suppressant)
Guaifenesin (Expectorant)- •
- Controls Cough
- •
- Relieves Chest Congestion
- •
- Thins & Loosens Mucus
Sugar-Free
No Added Alcohol
Specially
Formulated
for DIABETICS
Cherry Menthol FlavorFor Ages 12 & Over
8 FL OZ (237 ml)*This product is not manufactured or distributed by GSK Consumer Healthcare, owner of the registered trademark DYE-FREE Sugar-Free Adult Robitussin Cough+chest Congestion DM.
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INGREDIENTS AND APPEARANCE
WALGREEN ADULT COUGH PLUS CHEST CONGESTION DM
dextromethorphan hydrobromide and guaifenesin solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-7440 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE 20 mg in 20 mL GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN 200 mg in 20 mL Inactive Ingredients Ingredient Name Strength ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) EDETATE DISODIUM (UNII: 7FLD91C86K) GLYCERIN (UNII: PDC6A3C0OX) POTASSIUM CITRATE (UNII: EE90ONI6FF) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) WATER (UNII: 059QF0KO0R) SODIUM BENZOATE (UNII: OJ245FE5EU) SUCRALOSE (UNII: 96K6UQ3ZD4) XANTHAN GUM (UNII: TTV12P4NEE) Product Characteristics Color RED Score Shape Size Flavor CHERRY Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-7440-08 1 in 1 CARTON 11/01/2022 1 237 mL in 1 BOTTLE; Type 1: Convenience Kit of Co-Package Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M012 11/01/2022 Labeler - WALGREEN COMPANY (008965063)