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Allertness Aid

Dosage form: tablet
Ingredients: CAFFEINE 200mg
Labeler: Select Corporation
NDC Code: 52904-470

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Facts

Active Ingredients Caffeine 200mg

Alertness Aid

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

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 Caffeine warning: The
recommended dose of this product contains about as much
caffeine as a 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 heart beat.
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.

Inactive
Ingredients: carnauba wax, colloidal silicon
dioxide, dextrates, hypromellose, magnesium stearate,
microcrystalline cellulose, polyethylene glycol, titanium
dioxide

MM1

ALLERTNESS AID  
caffeine tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52904-470
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CAFFEINE (CAFFEINE) CAFFEINE200 mg
Inactive Ingredients
Ingredient NameStrength
TITANIUM DIOXIDE 
SILICON DIOXIDE 
CARNAUBA WAX 
POLYETHYLENE GLYCOL 300 
CELLULOSE, MICROCRYSTALLINE 
MAGNESIUM STEARATE 
DEXTRATES 
Product Characteristics
Colorwhite (snow white) Scoreno score
ShapeROUND (TCL363) Size11mm
FlavorImprint CodeTCL363
Contains    
Packaging
#Item CodePackage Description
1NDC:52904-470-022 TABLET (TABLET) in 1 PACKET
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34010/15/2012
Labeler - Select Corporation (053805599)
Registrant - Select Corporation (053805599)

 
Select Corporation

Medically reviewed on Oct 15, 2018

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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