NDC | 63868-855-52 |
Set ID | 910fae95-086e-4b37-b4ae-b2b286eafb74 |
Category | HUMAN OTC DRUG LABEL |
Packager | QUALITY CHOICE (Chain Drug Marketing Association) |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART341 |
- Active ingredients (in each 5 mL, 1 teaspoon)
- 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
- this adult product is not intended for use in children under 12 years of age
- measure only with dosing cup provided
- keep dosing cup with product
- tsp = teaspoon, mL = milliliter
age dose adults and children 12 years and over 2 tsp (10 mL) every 4 hours children under 12 years do not use - Other information
- Inactive ingredients
-
Principal Display Panel
*Compare to the active ingredients in Robitussin®
Sugar-Free
Non-Drowsy
Tussin DM
Cough & Chest Congestion
Dextromethorphan HBr Cough Suppressant
Guaifenesin Expectorant
Relieves:
Cough
Mucus
For Ages 12 & Over
Alcohol Free
DM Sugar-Free Formula Specially Formulated for Diabetic Use
FL OZ (mL)
*This product is not manufactured or distributed by Pfizer Consumer Healthcare, distributors of Robitussin® Peak Cold Sugar-Free Cough & Chest Congestion DM.
TAMPER EVIDENT: DO NOT USE IF SAFETY SEAL ON THE BOTTLE OR UNDER THE CAP IS BROKEN OR MISSING.
Distributed by C.D.M.A., Inc.
43157 W. Nine Mile
Novi, MI 48376-0995
www.qualitychoice.com
Questions: 248-449-9300
PARENTS: Learn about teen medicine abuse www.StopMedicineAbuse.org
- Package Label
-
INGREDIENTS AND APPEARANCE
TUSSIN DM SUGAR FREE
dextromethorphan hbr, guaifenesin liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63868-855 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE 10 mg in 5 mL GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN 100 mg in 5 mL Inactive Ingredients Ingredient Name Strength ACESULFAME POTASSIUM (UNII: 23OV73Q5G9) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) GLYCERIN (UNII: PDC6A3C0OX) METHYLPARABEN (UNII: A2I8C7HI9T) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) POVIDONE (UNII: FZ989GH94E) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) WATER (UNII: 059QF0KO0R) SACCHARIN SODIUM (UNII: SB8ZUX40TY) SODIUM BENZOATE (UNII: OJ245FE5EU) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63868-855-52 1 in 1 BOX 05/30/2014 12/30/2021 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 FINAL part341 05/30/2014 12/30/2021 Labeler - QUALITY CHOICE (Chain Drug Marketing Association) (011920774)