Label: QCH ADULT TUSSIN DM SUGAR FREE 545- dextromethorphan hbr, guaifenesin liquid
- NDC Code(s): 83324-025-04
- Packager: Chain Drug Marketing Association Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated May 8, 2024
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT(S)
- PURPOSE
- USE(S)
- 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
- STOP USE AND ASK DOCTOR IF
- IF PREGNANT OR BREAST-FEEDING,
- KEEP OUT OF REACH OF CHILDREN.
-
DIRECTIONS
- shake well before using
- 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 & children 12 years & over 20 mL every 4 Hours Children under 12 years do not use - OTHER INFORMATION
- INACTIVE INGRADIENTS
-
PRINCIPAL DISPLAY PANEL
NDC 83324-025-04
QUALITY CHOICE
* Compare to the Active Ingredients in Robitussin® DM
Adult Tussin DM
Cough Suppressant/ Expectorant
Dextromethorphan HBr 20 mg per 20 mL
Guaifenesin 200 mg per 20 mL
For Ages 12 & Over
Helps Control Cough
Relieves Chest Congestion
Thins and Loosens Mucus
Specially Formulated for Diabetics
Non-Drowsy
Sugar Free Dye Free
Peppermint Flavor
4 FL OZ (118 mL)
-
INGREDIENTS AND APPEARANCE
QCH ADULT TUSSIN DM SUGAR FREE 545
dextromethorphan hbr, guaifenesin liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83324-025 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 CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) GLYCERIN (UNII: PDC6A3C0OX) MENTHOL (UNII: L7T10EIP3A) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) WATER (UNII: 059QF0KO0R) SODIUM BENZOATE (UNII: OJ245FE5EU) SODIUM CITRATE (UNII: 1Q73Q2JULR) SORBITOL (UNII: 506T60A25R) SUCRALOSE (UNII: 96K6UQ3ZD4) XANTHAN GUM (UNII: TTV12P4NEE) Product Characteristics Color Score Shape Size Flavor PEPPERMINT Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83324-025-04 1 in 1 CARTON 05/08/2024 1 118 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 part341 05/08/2024 Labeler - Chain Drug Marketing Association Inc. (011920774) Establishment Name Address ID/FEI Business Operations Guardian Drug Company 119210276 MANUFACTURE(83324-025)