Label: FOSTER AND THRIVE ADULT TUSSIN DM- dextromethorphan hydrobromide, guaifenesin solution
- NDC Code(s): 70677-1035-1, 70677-1035-2
- Packager: Strategic Sourcing Services LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 25, 2023
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- Official Label (Printer Friendly)
- Active ingredients (in each 20 mL)
- Purposes
- Uses
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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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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
- •
- 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
- Other information
- Inactive ingredients
- Questions or comments?
-
Package/Label Principal Display Panel
COMPARE TO ROBITUSSIN® COUGH + CHEST CONGESTION DM
ACTIVE INGREDIENTS
Foster & Thrive™
Adult Tussin DM
Dextromethorphan HBr
Guaifenesin
COUGH SUPPRESSANT
EXPECTORANT
Cough & Chest Congestion DM
For Ages 12 & Over
Non-Drowsy**
Alcohol-Free | Gluten Free
Relieves:
• Cough
• Mucus
SEE NEW DOSING
RASPBERRY FLAVOR
DOSING CUP INCLUDED
**WHEN TAKEN AS DIRECTED
4 FL OZ (118 mL)
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INGREDIENTS AND APPEARANCE
FOSTER AND THRIVE ADULT TUSSIN DM
dextromethorphan hydrobromide, guaifenesin solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70677-1035 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) FD&C RED NO. 40 (UNII: WZB9127XOA) GLYCERIN (UNII: PDC6A3C0OX) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) WATER (UNII: 059QF0KO0R) SODIUM BENZOATE (UNII: OJ245FE5EU) SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR) SORBITOL (UNII: 506T60A25R) SUCRALOSE (UNII: 96K6UQ3ZD4) XANTHAN GUM (UNII: TTV12P4NEE) Product Characteristics Color RED Score Shape Size Flavor FRUIT Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70677-1035-1 1 in 1 CARTON 10/25/2023 1 118 mL in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:70677-1035-2 1 in 1 CARTON 10/25/2023 2 237 mL in 1 BOTTLE; 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 10/25/2023 Labeler - Strategic Sourcing Services LLC (116956644)