ALLERTNESS AID caffeine tablet

Land: Verenigde Staten

Taal: Engels

Bron: NLM (National Library of Medicine)

Werkstoffen:

CAFFEINE (UNII: 3G6A5W338E) (CAFFEINE - UNII:3G6A5W338E)

Beschikbaar vanaf:

Chain Drug Consortium

INN (Algemene Internationale Benaming):

CAFFEINE

Samenstelling:

CAFFEINE 200 mg

Prescription-type:

OTC DRUG

Autorisatie-status:

OTC monograph not final

Productkenmerken

ALLERTNESS AID- CAFFEINE TABLET
CHAIN DRUG CONSORTIUM
_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 INGREDIENT
Caffeine 200 mg
PURPOS E
Alertness aid
US ES
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
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 a cup of coffee.
_STOP USE AND ASK A DOCTOR IF_
fatigue or drowsiness persists or continues to occur . For occasional
use only.
_IF PREGNANCY OR BREAST-FEEDING_
ask a health professional before use.
KEEP OUT OF REACH OF CHILDREN
In case of accidental overdose, contact a doctor or Poison Control
Center right away.
DIRECTIONS
Adults and children 12 years of age and older: take 1 tablet not more
often than every 3 to 4 hours
Children under 12 years of age: Do not use
INACTIVE INGREDIENTS
colloidal silicon dioxide, croscarmellose sodium, D&C yellow #10,
dicalcium phosphate dihydrate,
FD&C yellow #6, hydroxypropyl methylcellulose, magnesium stearate,
microcrystalline cellulose,
propylene glycol, titanium dioxide, triacetin
PACKAGE/LABEL PRINCIPAL DISPLAY PANEL
ALLERTNESS AID
caffeine tablet
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:6 8 0 16 -19 5
ROUTE OF ADMINISTRATION
ORAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRE NG TH
CAFFEINE (UNII: 3G6 A5W338 E) (CAFFEINE - UNII:3G6 A5W338 E)
CAFFEINE
20 0 mg
INACTIVE INGREDIENTS
INGREDIENT NAME
STRE NG TH
Chain Drug Consortium
SILICO N DIO XIDE (UNII: ETJ7Z6 XBU4)
CRO SCARMELLO SE SO DIUM (UNII: M28 OL1HH48 )
D&C YEL