Label: STAY AWAKE- caffeine tablet
- NDC Code(s): 41163-226-10
- Packager: United Natural Foods, Inc. dba UNFI
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated September 20, 2023
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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
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- Inactive ingredients
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Principal Display Panel
EQUALINE®
compare to Vivarin® active ingredient*
NDC 41163-226-10maximum strength
stay awake
caffeine 200 mg (alertness aid)
• helps restore alertness
• equal to about one cup of coffee40 tablets
actual size
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 Meda AB, owner of the
registered trademark Vivarin®.
50844 REV1219E22610DISTRIBUTED BY UNFI
PROVIDENCE, RI 02908 USA
855-423-2630Equaline 44-226
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INGREDIENTS AND APPEARANCE
STAY AWAKE
caffeine tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:41163-226 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 (UNII: H77VEI93A8) 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:41163-226-10 5 in 1 CARTON 11/21/1996 1 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 - United Natural Foods, Inc. dba UNFI (943556183) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 038154464 pack(41163-226) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 832867837 manufacture(41163-226) , pack(41163-226) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 967626305 pack(41163-226) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 117025878 manufacture(41163-226)