Label: ALLERTNESS AID- caffeine tablet
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Contains inactivated NDC Code(s)
NDC Code(s): 52904-470-02 - Packager: Select Corporation
- Category: HUMAN OTC DRUG LABEL
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 Label Information
Updated October 15, 2012
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- DOSAGE & ADMINISTRATION
- INDICATIONS & USAGE
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WARNINGS
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. - PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ALLERTNESS AID
caffeine tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:52904-470 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CAFFEINE (UNII: 3G6A5W338E) (CAFFEINE - UNII:3G6A5W338E) CAFFEINE 200 mg Inactive Ingredients Ingredient Name Strength TITANIUM DIOXIDE (UNII: 15FIX9V2JP) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) CARNAUBA WAX (UNII: R12CBM0EIZ) POLYETHYLENE GLYCOL 300 (UNII: 5655G9Y8AQ) CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U) MAGNESIUM STEARATE (UNII: 70097M6I30) DEXTRATES (UNII: G263MI44RU) Product Characteristics Color white (snow white) Score no score Shape ROUND (TCL363) Size 11mm Flavor Imprint Code TCL363 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:52904-470-02 2 in 1 PACKET Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part340 10/15/2012 Labeler - Select Corporation (053805599) Registrant - Select Corporation (053805599)