NDC | 49348-861-34, 49348-861-37 |
Set ID | aa0d2151-51c6-4ba0-8719-75941559f553 |
Category | HUMAN OTC DRUG LABEL |
Packager | Strategic Sourcing Services LLC |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART341 |
- Active ingredients (in each 10 mL)
- Purposes
- Uses
-
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
- •
- cough that occurs with too much phlegm (mucus)
- •
- cough that lasts or is chronic such as occurs with smoking, asthma, chronic bronchitis, or emphysema
-
Directions
- •
- do not take more than 6 doses in any 24-hour period
- •
- measure only with dosing cup provided
- •
- keep dosing cup with product
- •
- 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
10 mL
every 4 hours
children under 12 years
do not use
- Other information
- Inactive ingredients
- Questions or comments?
-
Principal Display Panel
COMPARE TO ROBITUSSIN® SUGAR-FREE COUGH + CHEST CONGESTION DM ACTIVE INGREDIENTS
Sugar-Free
Adult tussin DM
Cough Suppressant (Dextromethorphan HBr)
Expectorant (Guaifenesin)
Cough & Chest Congestion DM
Specially formulated for diabetics
Relieves:
Cough
Mucus
For ages 12 & over
Alcohol-free
NON-DROWSY
GLUTEN FREE
4 FL OZ (118 mL)
-
INGREDIENTS AND APPEARANCE
SUNMARK TUSSIN DM SUGAR FREE
dextromethorphan hbr, guaifenesin solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49348-861 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 10 mL GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN 200 mg in 10 mL Inactive Ingredients Ingredient Name Strength ASPARTAME (UNII: Z0H242BBR1) BENZOIC ACID (UNII: 8SKN0B0MIM) GLYCERIN (UNII: PDC6A3C0OX) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) WATER (UNII: 059QF0KO0R) MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) Product Characteristics Color Score Shape Size Flavor CHERRY Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49348-861-34 1 in 1 CARTON 06/24/2003 1 118 mL in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:49348-861-37 1 in 1 CARTON 06/24/2003 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 final part341 06/24/2003 Labeler - Strategic Sourcing Services LLC (116956644)