Label: DAYTIME COUGH NON DROWSY- dextromethorphan hydrobromide solution
- NDC Code(s): 41250-473-38, 41250-473-40
- Packager: Meijer Distribution Inc
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated November 3, 2021
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- Official Label (Printer Friendly)
- Active ingredient (in each 15 mL)
- Purpose
- Use
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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
- •
- cough that occurs with too much phlegm (mucus)
- •
- persistent or chronic cough such as occurs with smoking, asthma, or emphysema
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
- Principal Display Panel
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INGREDIENTS AND APPEARANCE
DAYTIME COUGH NON DROWSY
dextromethorphan hydrobromide solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:41250-473 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE 15 mg in 15 mL Inactive Ingredients Ingredient Name Strength ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) D&C YELLOW NO. 10 (UNII: 35SW5USQ3G) FD&C YELLOW NO. 6 (UNII: H77VEI93A8) HIGH FRUCTOSE CORN SYRUP (UNII: XY6UN3QB6S) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) WATER (UNII: 059QF0KO0R) SACCHARIN SODIUM (UNII: SB8ZUX40TY) SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR) Product Characteristics Color ORANGE (light) Score Shape Size Flavor CITRUS (blend) Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:41250-473-38 296 mL in 1 BOTTLE; Type 0: Not a Combination Product 08/15/2007 07/13/2014 2 NDC:41250-473-40 355 mL in 1 BOTTLE; Type 0: Not a Combination Product 12/12/2012 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part341 08/15/2007 Labeler - Meijer Distribution Inc (006959555)