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Stay awake - Medication Information

Product NDC Code 70677-0021
Drug Name

Stay awake

Type Brand
Pharm Class Central Nervous System Stimulant [EPC],
Central Nervous System Stimulation [PE],
Methylxanthine [EPC],
Xanthines [CS]
Active Ingredients
Caffeine 200 mg/1
Route ORAL
Dosage Form TABLET
RxCUI drug identifier 198520
Application Number M011
Labeler Name Strategic Sourcing Services LLC
Packages
Package NDC Code Description
70677-0021-1 2 blister pack in 1 carton (70677-0021-1) / 8 tablet in 1 blister pack
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredient (in each tablet) Caffeine 200 mg

Dosage and administration

Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.
Directions adults and children 12 years and over: take 1 tablet not more often than every 3 to 4 hours children under 12 years: do not use

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients corn starch, D&C yellow #10 aluminum lake, dextrates hydrated, dibasic calcium phosphate dihydrate, FD&C yellow #6 aluminum lake, magnesium stearate, microcrystalline cellulose, silicon dioxide

Indications and usage

A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.
Use helps restore mental alertness or wakefulness when experiencing fatigue or drowsiness

Purpose

Information about the drug product’s indications for use.
Purpose Alertness aid

Spl product data elements

Usually a list of ingredients in a drug product.
stay awake caffeine CAFFEINE CAFFEINE STARCH, CORN D&C YELLOW NO. 10 ALUMINUM LAKE DEXTROSE MONOHYDRATE DIBASIC CALCIUM PHOSPHATE DIHYDRATE FD&C YELLOW NO. 6 MAGNESIUM STEARATE MICROCRYSTALLINE CELLULOSE SILICON DIOXIDE 44;226

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
Principal Display Panel sun mark® COMPARE TO VIVARIN® ACTIVE INGREDIENT* NDC 70677-0021-1 stay awake CAFFEINE 200 mg Alertness Aid Equal to about a cup of coffee 16 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 REV1219B22621 Distributed by McKesson Corp., via SSSL Memphis, TN 38141 © 2003 McKesson Corporation www.sunmarkbrand.com Money Back Guarantee Rev. 01/22 SunMark 44-226 SunMark 44-226

Spl unclassified section

Information not classified as belonging to one of the other fields. Approximately 40% of labeling with effective_time between June 2009 and August 2014 have information in this field.
Other information each tablet contains: calcium 35 mg TAMPER EVIDENT: DO NOT USE IF OUTER PACKAGE IS OPENED OR BLISTER IS TORN OR BROKEN store at 25ºC (77ºF); excursions permitted between 15º-30ºC (59º-86ºF) see end flap for expiration date and lot number

Do not use

Information about all contraindications for use. These contraindications are absolute and are intended for situations in which consumers should not use the product unless a prior diagnosis has been established by a doctor or for situations in which certain consumers should not use the product under any circumstances regardless of whether a doctor or health professional is consulted.
Do not use for children under 12 years of age as a substitute for sleep

Keep out of reach of children

Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Questions

A telephone number of a source to answer questions about a drug product. Sometimes available days and times are also noted.
Questions or comments? 1-800-426-9391

Stop use

Information about when use of the drug product should be discontinued immediately and a doctor consulted. Includes information about any signs of toxicity or other reactions that would necessitate immediately discontinuing use of the product.
Stop use and ask a doctor if fatigue or drowsiness persists or continues to recur.

Pregnancy or breast feeding

Pregnancy or Breast feeding
If pregnant or breast-feeding, ask a health professional before use.

Warnings

Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.
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. Do not use for children under 12 years of age as a substitute for sleep Stop use and ask a doctor if fatigue or drowsiness persists or continues to recur. If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API