NDC | 59779-031-02, 59779-668-40 |
Set ID | 4d6df7fa-33ed-4715-98fb-f35bd424b30a |
Category | HUMAN OTC DRUG LABEL |
Packager | CVS Pharmacy |
Generic Name | |
Product Class | Antihistamine |
Product Number | |
Application Number | PART341 |
- Active ingredients (in each 30 mL) - Nighttime Cough
- Purpose - Nighttime Cough
- Uses – Nighttime Cough
- Warnings
-
Do not use – Nighttime Cough
- •
- 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 – Nighttime Cough
- Ask a doctor or pharmacist before use if you are – Nighttime Cough
- When using this product – Nighttime Cough
- Stop use and ask a doctor if - Nighttime Cough
- If pregnant or breast-feeding, - Nighttime Cough
- Keep out of reach of children. - Nighttime Cough
- Directions – Nighttime Cough
- Other information – Nighttime Cough
- Inactive ingredients – Nighttime Cough
- Questions or comments – Nighttime Cough
- Active ingredient (in each 15 mL) - Daytime Cough
- Purpose - Daytime Cough
- Uses – Daytime Cough
- Warnings
-
Do not use – Daytime Cough
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 – Daytime Cough
- Stop use and ask a doctor if – Daytime Cough
- If pregnant or breast-feeding, - Daytime Cough
- Keep out of reach of children. – Daytime Cough
- Directions – Daytime Cough
- Other information – Daytime Cough
- Inactive ingredients – Daytime Cough
- Questions or comments? – Daytime Cough
-
Principal Display Panel – Nighttime Cough
DAY & NIGHT COMBO PACK
Compare to the active ingredient in Vicks® DayQuil® Cough
Cough Relief
Non-Drowsy
Daytime Cough
DEXTROMETHORPHAN HBr
Cough suppressant
Powerful cough relief for up to 8 hours
Antihistamine free
Alcohol free
Citrus Blend Flavor
Compare to the active ingredients in Vicks® NyQuil® Cough
Cough Relief
Nighttime Cough
DEXTROMETHORPHAN HBr
Cough suppressant
DOXYLAMINE SUCCINATE
Antihistamine
Relieves:
Cough
Sneezing
Runny nose
ALCOHOL 10%
Cherry Flavor
TWO 12 FL OZ (355 mL) UNITS TOTAL 24 FL OZ (1.5 PT) (710 mL)
-
INGREDIENTS AND APPEARANCE
DAYTIME COUGH NIGHTTIME COUGH
dextromethorphan hbr, doxylamine succinate kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59779-031 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59779-031-02 1 in 1 CARTON; Type 0: Not a Combination Product 08/07/2012 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 1 BOTTLE 355 mL Part 2 1 BOTTLE 355 mL Part 1 of 2 NIGHTTIME COUGH
dextromethorphan hydrobromide, doxylamine succinate solutionProduct Information Item Code (Source) NDC:59779-668 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE 30 mg in 30 mL DOXYLAMINE SUCCINATE (UNII: V9BI9B5YI2) (DOXYLAMINE - UNII:95QB77JKPL) DOXYLAMINE SUCCINATE 12.5 mg in 30 mL Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) FD&C RED NO. 40 (UNII: WZB9127XOA) HIGH FRUCTOSE CORN SYRUP (UNII: XY6UN3QB6S) POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) WATER (UNII: 059QF0KO0R) SACCHARIN SODIUM (UNII: SB8ZUX40TY) SODIUM CITRATE (UNII: 1Q73Q2JULR) Product Characteristics Color RED (Dark Red) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59779-668-40 355 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 09/23/2002 Part 2 of 2 DAYTIME COUGH
dextromethorphan hbr solutionProduct Information 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 (UNII: 3WJQ0SDW1A) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) WATER (UNII: 059QF0KO0R) SACCHARIN SODIUM (UNII: SB8ZUX40TY) SODIUM CITRATE (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 1 355 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 08/07/2012 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part341 08/07/2012 Labeler - CVS Pharmacy (062312574)