Drowz Away description, usages, side effects, indications, overdosage, supplying and lots more!

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Drowz Away

Care One (American Sales Company)
P and L Development of New York Corporation

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient (in each tablet)

Caffeine 200 mg

Purpose

Alertness aid

Use

  • helps restore mental alertness or wakefulness when experiencing fatigue or drowsiness

Warnings

  • the recommended dose of this product contains about as much caffeine as one cup of coffee.  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. 
  • For occasional use only. Not intended for use as a substitute for sleep
  • do not give to children under 12 years of age

Stop use and ask a doctor if

fatigue or drowsiness persists or continues to recur

If pregnant or breast-feeding,

ask a health care professional before use.

Keep out of reach of children.

In case of overdose, get medical help or contact a Poison Control Center right away.

Directions

  • adults and children 12 years of age and over: take 1 tablet (200 mg) not more often than every 3 to 4 hours

Drowz Away Other information

  • each tablet contains: calcium 60 mg
  • store at controlled room temperature 15-30°C (59-86°F)
  • avoid excessive heat and humidity
  • * This product is not manufactured or distributed by Glaxosmithkline, owner of the registered trademark Vivarin®

Inactive ingredients

D&C Yellow #10 aluminum lake, dicalcium phosphate, FD&C Yellow #6 aluminum lake, magnesium stearate, microcrystalline cellulose and silica. May also contain: cellulose, croscarmellose sodium, sodium starch glycolate and starch

Principal Display Panel

compare to active ingredient in Vivarin® *

Maximum strength

DROWZ-AWAY

caffeine alertness aid

Each tablet contains 200 mg caffeine equal to about one cup of coffee

TAMPER EVIDENT- USE ONLY IF BLISTERS ARE INTACT

Distributed by: American Sales Company

4201 walden avenue, Lancaster, NY 14086

www.care1.com

Drowz Away
caffeine 200 mg

Drowz Away

Caffeine TABLET

Product Information

Product Type Human otc drug label Item Code (Source) NDC:41520-252
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
CAFFEINE 200 mg

Inactive Ingredients

Ingredient Name Strength
D&C YELLOW NO. 10
CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS
FD&C YELLOW NO. 6
MAGNESIUM STEARATE
cellulose, microcrystalline
SILICON DIOXIDE
POWDERED CELLULOSE
CROSCARMELLOSE SODIUM
sodium starch glycolate type a corn
STARCH, CORN

Product Characteristics

Color Size Imprint Code Shape
YELLOW 11 mm 212;212 ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 8 in 1 BLISTER PACK
2 NDC:41520-252-16 2 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part340 2010-08-31


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Be sure to consult your doctor before taking any medication!
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