Label: ALERT ALERTNESS AID- caffeine tablet
- NDC Code(s): 50844-226-12, 50844-226-21
- Packager: L.N.K. International, Inc.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated August 15, 2024
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- Official Label (Printer Friendly)
- Active ingredient (in each tablet)
- Purpose
- Uses
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Warnings
For occasional use only
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.
- Directions
- Other information
- Inactive ingredients
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Principal Display Panel
QUALITY
+PLUSNDC 50844-226-12
*Compare to active ingredient
in VIVARIN®ALERT TABLETS
Caffeine 200 mgALERTNESS AID
Equal to about a cup of coffee
100 Tablets
ACTUAL SIZE
TAMPER EVIDENT: DO NOT USE IF IMPRINTED
SAFETY SEAL UNDER CAP IS BROKEN OR MISSING
*This product is not manufactured or distributed by Vespyr Brands, Inc.,
owner of the registered trademark Vivarin®.50844 REV1219A22612
Distributed by LNK INTERNATIONAL, INC.
60 Arkay Drive
Hauppauge, NY 11788
USAQuality Plus 44-226
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INGREDIENTS AND APPEARANCE
ALERT ALERTNESS AID
caffeine tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50844-226 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 STARCH, CORN (UNII: O8232NY3SJ) D&C YELLOW NO. 10 ALUMINUM LAKE (UNII: CQ3XH3DET6) DEXTROSE MONOHYDRATE (UNII: LX22YL083G) DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP) FD&C YELLOW NO. 6 ALUMINUM LAKE (UNII: GYP6Z2JR6Q) MAGNESIUM STEARATE (UNII: 70097M6I30) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) Product Characteristics Color yellow Score no score Shape ROUND Size 11mm Flavor Imprint Code 44;226 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50844-226-12 100 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/21/1996 2 NDC:50844-226-21 2 in 1 CARTON 11/21/1996 03/04/2022 2 8 in 1 BLISTER PACK; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M011 11/21/1996 Labeler - L.N.K. International, Inc. (038154464) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 038154464 pack(50844-226) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867837 manufacture(50844-226) , pack(50844-226) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 967626305 pack(50844-226) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 117025878 manufacture(50844-226)