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Stay Awake drug information

CAFFEINE
United Natural Foods, Inc. dba UNFI · ORAL

Product NDC: 41163-226

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Source label information, not individualized medical advice. This record applies to the product and labeler shown below. Compare the exact formulation, strength and country with your package and the current source label.
Generic nameCAFFEINE
Labeler / manufacturerUnited Natural Foods, Inc. dba UNFI
RouteORAL
Drug classCentral Nervous System Stimulant / Methylxanthine
Product NDC41163-226
Label effective date2026-08-21

Official product label reference

Stay Awake — United Natural Foods, Inc. dba UNFI

This page contains 12 source sections for CAFFEINE, oral route. Label set 15e4d040-ed21-46e7-98c6-56267f388f57, version 18.

Retrieved 2026-10-02 · openFDA dataset updated 2026-10-02 · Check the current DailyMed label

Label records can cover multiple strengths or package sizes. A label listing does not by itself establish FDA approval or current market availability. Check the source and application history for this specific product.

Uses described in the label

Use helps restore mental alertness or wakefulness when experiencing fatigue or drowsiness

Purpose

Purpose Alertness aid
Dosage and administration — label text
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
Warnings
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.
Active ingredient
Active ingredient (in each tablet) Caffeine 200 mg
Do not use
Do not use for children under 12 years of age as a substitute for sleep
When to stop use and seek help
Stop use and ask a doctor if fatigue or drowsiness persists or continues to recur.
Pregnancy or breast feeding
If pregnant or breast-feeding, ask a health professional before use.
Child safety
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
Storage and handling
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 25°C (77°F); excursions permitted between 15°-30°C (59°-86°F) see end flap for expiration date and lot number
Inactive ingredient
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
Questions
Questions or comments? 1-855-423-2630

Official sources and product identifiers

Substances listed: CAFFEINE

RxNorm identifiers: 198520

Package NDC codes

41163-226-10

Further research and background

These are external searches for related information. Research, encyclopedia and news articles have not been imported into this product record.

Coverage and corrections

The text is extracted from a US structured product label. Tables are represented as text where supplied; formatting and illustrations may be lost. A missing section does not mean a risk is absent. This reference has not been independently reviewed by a clinician and is not a live safety-alert service.

Source retrieved 2026-10-02. Read the source policy.