Indications and uses
Helps restore mental alertness or wakefulness when experiencing fatigue or drowsiness
Uplift Chewable
- Manufacturer
- Carolina Cannabis Creations LLC
- Effective date
- 2025-01-15
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-06-01 00:52:45
Label at a glance#
ProductUplift Chewable
Active ingredientCAFFEINE
Label structure7 sections
Dosage and administration
Adults 18 years of age and over: take up to 2 chewables every 4 to 6 hours, not more that 4 chewable in 24 hours. Do not swallow whole
Label contents#
Full prescribing information#
Active ingredients (in each chewable)
Caffeine 50mg
Purpose
Alertness aid
Uses
Helps restore mental alertness or wakefulness when experiencing fatigue or drowsiness
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, food, or beverages while taking this product because too much caffeine may cause nervousness, sleeplessness, and occasionally, rapid heartbeat.
Do not use
as a substitute for sleep, or in children under 12 years of age.
Ask a doctor before use if you are
Presently taking a prescription drug
Ask a doctor before use if you are
Presently taking a prescription drug
Stop using and ask a doctor if
fatigue or drowsiness persists or continues to recur
If pregnant or breast-feeding
consult a health professional before use
Keep out of reach of children
In case of overdose seek medical help or contact a poison control center right away
Keep out of reach of children
In case of overdose, seek medical help or contact a poison control center right away
Directions
Adults 18 years of age and over: take up to 2 chewables every 4 to 6 hours, not more that 4 chewable in 24 hours.
Do not swallow whole
Other information
Store at 68-77 degrees F
Avoid direct sunlight
Inactive ingredients
Artificial flavors, Citric acid, Gelatin, Hexahydrocannabinol, Light corn syrup, Potassium Sorbate, Sorbitol, Beet root powder, Sugar, Water.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed Pharmacologic Classes#
| Class | Version | Type | Effective |
|---|---|---|---|
| CAFFEINE Pharmacologic Class Indexing | 2 | Indexing - Pharmacologic Class | 20180813 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 82876-833-20 | Uplift Chewable | 108.27 g in 1 BAG | CHEWABLE GEL | 108.27 | 2 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Uplift Chewable
- Caffeine
- SUCROSE
- SORBITOL
- GELATIN
- HEXAHYDROCANNABINOL
- ANHYDROUS CITRIC ACID
- POTASSIUM SORBATE
- BETA VULGARIS ROOT FRUCTOOLIGOSACCHARIDES
- CORN SYRUP
- WATER
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 82876-833 | 82876-833-20 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| SUCROSE | C151H8M554 | IACT |
| SORBITOL | 506T60A25R | IACT |
| GELATIN | 2G86QN327L | IACT |
| HEXAHYDROCANNABINOL | D4K2ZLP4DT | IACT |
| CAFFEINE | 3G6A5W338E | ACTIB |
| ANHYDROUS CITRIC ACID | XF417D3PSL | IACT |
| POTASSIUM SORBATE | 1VPU26JZZ4 | IACT |
| BETA VULGARIS ROOT FRUCTOOLIGOSACCHARIDES | N2UDM48ZD6 | IACT |
| CORN SYRUP | 9G5L16BK6N | IACT |
| WATER | 059QF0KO0R | IACT |
Source Document#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Uplift Chewable | CAFFEINE | Carolina Cannabis Creations LLC | 04a71dd1-19ae-d1cd-e063-6294a90a4fc0 | 2025-01-15 | Warnings | 82876-833-20 82876-833 82876083320 2bcaad44-2492-020e-e063-6294a90a955b 04a71dd1-19ae-d1cd-e063-6294a90a4fc0 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.