Label: STAY AWAKE- caffeine tablet
- NDC Code(s): 50804-262-10, 50804-262-21
- Packager: Geiss, Destin & Dunn Inc.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated July 8, 2024
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- Active ingredient (in each tablet)
- Purpose
- Use
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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
GOODSENSE®
NDC 50804-262-10
Stay Awake
Caffeine
Alertness Aid40Tablets - 200 mg Each
actual size
*Compare to the active ingredient of
Vivarin®TAMPER EVIDENT: DO NOT USE IF PACKAGE
IS OPENED OR IF BLISTER UNIT IS TORN,
BROKEN OR SHOWS ANY SIGNS OF TAMPERING*This product is not manufactured or distributed by Vespyr
Brands, Inc., owner of the registered trademark Vivarin®.
50844 REV1219C22610Distributed by:
Perrigo Direct, Inc., Peachtree City, GA 30269
www.PerrigoDirect.com (1-800-426-9391)
GoodSense® is a registered trademark of
L. Perrigo Company.Good Sense 44-226
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INGREDIENTS AND APPEARANCE
STAY AWAKE
caffeine tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50804-262 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:50804-262-21 2 in 1 CARTON 07/01/2020 1 8 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:50804-262-10 5 in 1 CARTON 07/01/2020 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 07/01/2020 Labeler - Geiss, Destin & Dunn Inc. (076059836) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 038154464 pack(50804-262) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867837 manufacture(50804-262) , pack(50804-262) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 967626305 pack(50804-262) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 117025878 manufacture(50804-262)