Alert
CAFFEINE
ORAL
HUMAN OTC DRUG
Alert is an FDA drug label for the active ingredient CAFFEINE manufactured by Time Cap Labs, Inc administered by ORAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20181217.
- Generic name
- CAFFEINE
- Manufacturer
- Time Cap Labs, Inc
- Product type
- HUMAN OTC DRUG
- Route
- ORAL
- Dosage form
- N/A
- NDC
- 49483-343
- Application
- part340
- Label effective
- 20181217
Active ingredients
Active ingredient (in each tablet) Caffeine 200 mg
Indications & Usage
Uses helps restore mental alertness or wakefulness when experiencing fatigue or drowsiness
Dosage & Administration
Directions adults and children 12 years and over: take 1 tablet not more often than every 3 to 4 hours
Contraindications
Not available.
Warnings
Warnings For occasional use only
Adverse Reactions
Not available.