Sunmark stay awake description, usages, side effects, indications, overdosage, supplying and lots more!

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Sunmark stay awake

McKesson

McKesson Stay Awake Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient (in each tablet)

Caffeine 200 mg

Purpose

Alertness aid

Sunmark stay awake Uses

helps restore mental alertness or wakefulness when experiencing fatigue or drowsiness

Warnings

For occasional use only

Do not use

  • in children under 12 years of age
  • as a substitute for sleep

When using this product

limit the use of caffeine-containing medications, foods, or beverages while taking this product because too much caffeine may cause nervousness, irritability, sleeplessness, and occasionally, rapid heartbeat. The recommended dose of this product contains about as much caffeine as two cups of coffee.

Stop use and ask a doctor if

fatigue or drowsiness persists or continues to recur

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

adults and children 12 years of age and over: take 1 tablet not more often than every 3 to 4 hours

Sunmark stay awake Other information

  • store at 20-25°C (68-77°F)

Inactive ingredients

colloidal silicon dioxide, D&C yellow #10 aluminum lake, dextrose, FD&C yellow #6 aluminum lake, magnesium stearate, maltodextrin, microcrystalline cellulose, pregelatinized starch

Questions or comments? 1-800-719-9260

Principal Display Panel

COMPARE TO VIVARIN® ACTIVE INGREDIENT

stay awake

SAFE AND EFFECTIVE - as reported by a government appointed panel of experts.

Use as directed.

Safe as coffee

Alertness Aid

Each tablet contains 200 mg caffeine, equal to about two cups of coffee.

HELPS RESTORE ALERTNESS

GLUTEN FREE

200 mg

Sunmark stay awake
Stay Awake Carton Image 1 Stay Awake Carton Image 2

Sunmark stay awake

Caffeine TABLET

Product Information

Product Type Human otc drug label Item Code (Source) NDC:49348-771
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
CAFFEINE 200 mg

Inactive Ingredients

Ingredient Name Strength
DEXTROSE
MAGNESIUM STEARATE
cellulose, microcrystalline
SILICON DIOXIDE
maltodextrin

Product Characteristics

Color Size Imprint Code Shape
YELLOW 11 mm L409 ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 8 in 1 BLISTER PACK
2 NDC:49348-771-03 2 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part340 2003-08-21


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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