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day time nitetime cough

Meijer Distribution Inc

Meijer Distribution, Inc. Daytime Cough/Nite Time Cough Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient for Nighttime Cough (in each 15 ml tablespoon)

Dextromethorphan HBr 15 mg

Doxylamine succinate 6.25 mg

Purpose for Nighttime Cough

Cough suppressant

Antihistamine

Active ingredient for Daytime Cough (in each 15 ml tablespoon)

Dextromethorphan HBr 15 mg

Purpose for Daytime Cough

Cough suppressant

day time nitetime cough Uses

temporarily relieves:

  • cough due to minor throat and bronchial irritation
  • runny nose and sneezing (Nighttime Cough only)

 

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.
  • to make a child sleepy (Nighttime Cough only)

Ask a doctor before use if you have

  • cough that occurs with too much phlegm (mucus)
  • a breathing problem such as emphysema or chronic bronchitis
  • glaucoma
  • trouble urinating due to an enlarged prostate gland
  • persistent or chronic cough as occurs with smoking, asthma, or emphysema

Ask a doctor or pharmacist before use

if you are taking sedatives or tranquilizers

When using these products

  • do not use more than directed

In addition, when using Nighttime Cough:

  • may cause marked drowsiness
  • excitability may occur, especially in children
  • alcohol, sedatives and tranquilizers may increase drowsiness
  • be careful when driving a motor vehicle or operating machinery
  • avoid alcoholic drinks

Stop use and ask a doctor if

  • cough lasts for more than 7 days, comes back, or occurs with fever, rash or headache that lasts.

These could be signs of a serious condition.

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

In case of overdose, get medical help or contact a Poison Control Center right away. (1-800-222-1222)

Directions

  • take Nighttime Cough or Daytime Cough only as recommended
  • use dose cup
  • do not exceed 4 doses per 24 hours

Nighttime Cough

adults & children 12 yrs & over 30 ml (2 TBSP) every 6 hrs
children 4 to under 12 yrs ask a doctor
children under 4 yrs do not use

Daytime Cough

adults & children 12 yrs & over 30 ml (2 TBSP) every 6-8 hrs
children 6 to under 12 yrs 15 ml (1 TBSP) every 6-8 hrs
children 4 to under 6 yrs ask a doctor
children under 4 yrs do not use
  • when using other Daytime or Nighttime products, carefully read each label to insure correct dosing
  • each TBSP of Nighttime Cough contains: sodium 16 mg
  • each TBSP of Daytime Cough contains: sodium 13 mg

Inactive ingredients

Nighttime Cough

alcohol, anhydrous citric acid, FD&C blue # 1, FD&C red # 40, flavor, high fructose corn syrup, polyethylene glycol, propylene glycol, purified water, saccharin sodium, sodium citrate

Daytime Cough

anhydrous citric acid, D&C yellow # 10, FD&C yellow # 6, flavor, high fructose corn syrup, polyethylene glycol, propylene glycol, purified water, saccharin sodium, sodium citrate

Questions or comments? 

1-800-719-9260

Principal Display Panel for DayTime Cough

Compare to Vicks® DayQuil® Cough active ingredient

Non-Drowsy

Citrus Flavor

DayTime Cough

Cough Suppressant

All Day Cough Relief

up to 8 Hours

Dextromethorphan HBr - cough

Alcohol Free / Antihistamine Free

Principal Display Panel for NiteTime Cough

Compare to Vicks® NyQuil® Cough active ingredients

Cherry

NiteTime Cough

Cough Suppressant, Antihistamine

All Night Cough Relief

Dextromethorphan HBr - cough

Doxylamine Succinate - sneezing, runny nose

ALCOHOL 10%

day time nitetime cough
DayTime Cough/NiteTime Cough Package Image 1 DayTime Cough/NiteTime Cough Package Image 2

day time nitetime cough

dextromethorphan hbr, doxylamine succinate KIT

Product Information

Product Type Human otc drug label Item Code (Source) NDC:41250-031
Route of Administration DEA Schedule

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:41250-031-01 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part341 1992-01-10


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Be sure to consult your doctor before taking any medication!
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