FDA.reportPublic FDA data

NoSnooze

Manufacturer
Lil' Drug Store Products, Inc.
Effective date
2022-08-25
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
legacy-cache
Hydrated at
2026-08-01 21:54:55

Label at a glance#

ProductNoSnooze Circle K
Active ingredientCAFFEINE
Label structure13 sections

Dosage and administration

adults and children 12 years of age and older take 1 tablet (200 mg) not more often than every 3 to 4 hours children under 12 years of age do not use

Storage and handling

store at room temperature avoid excessive heat (greater than 100°F) and humidity do not use if inner pouch or carton is open or damaged see bottom panel for lot number and expiration date

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient (in each tablet)

OTC - ACTIVE INGREDIENT SECTION

Caffeine 200 mg

Purpose

OTC - PURPOSE SECTION

Alertness aid

Use

INDICATIONS & USAGE SECTION

helps restore mental alertness or wakefulness when experiencing fatigue or drowsiness

Warnings

WARNINGS SECTION

For occasional use only

Caffeine warning

SPL UNCLASSIFIED SECTION

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 heartbeat.

Do not use

OTC - DO NOT USE SECTION

  • in children under 12 years of age
  • as substitute for sleep

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • fatigue or drowsiness persists or continues to recur

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222).

Directions

DOSAGE & ADMINISTRATION SECTION

adults and children 12 years of age and oldertake 1 tablet (200 mg) not more often than every 3 to 4 hours
children under 12 years of agedo not use

Other information

STORAGE AND HANDLING SECTION

  • store at room temperature
  • avoid excessive heat (greater than 100°F) and humidity
  • do not use if inner pouch or carton is open or damaged
  • see bottom panel for lot number and expiration date

Inactive ingredients

INACTIVE INGREDIENT SECTION

croscarmellose sodium 1, colloidal silicon dioxide 1, D&C yellow #10 1, dicalcium phosphate dihydrate 1, FD&C blue #1 1, FD&C yellow #6 1, hypromellose 1, magnesium stearate, microcrystalline cellulose, polyethylene glycol 1, povidone 1, sodium starch glycolate 1, sucrose 1, titanium dioxide 1.

1 may contain

Questions or comments?

OTC - QUESTIONS SECTION

call toll-free 1-877-507-6516 (M-F 8AM-4:30PM CST)

SPL UNCLASSIFIED SECTION

Proudly distributed by Circle K Stores Inc.

PRINCIPAL DISPLAY PANEL - 200 mg Tablet Pouch Carton - 5830

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CIRCLE K ®

NoSnooze ™
Alertness Aid, Caffeine 200 mg

Maximum Strength

- Fast & Effective
- Safe as Coffee

6 Tablets
3 POUCHES, 2 TABLETS PER POUCH

PRINCIPAL DISPLAY PANEL - 200 mg Tablet Pouch Carton - 5830
PRINCIPAL DISPLAY PANEL - 200 mg Tablet Pouch Carton - 5830

PRINCIPAL DISPLAY PANEL - 200 mg Tablet Pouch Carton - 5930

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CIRCLE K ®

NoSnooze ™
Alertness Aid, Caffeine 200 mg

Maximum Strength

- Fast & Effective
- Safe as Coffee

6 Tablets
3 POUCHES, 2 TABLETS PER POUCH

PRINCIPAL DISPLAY PANEL - 200 mg Tablet Pouch Carton - 5930
PRINCIPAL DISPLAY PANEL - 200 mg Tablet Pouch Carton - 5930

PRINCIPAL DISPLAY PANEL - 200 mg Tablet Pouch Carton - 5530

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

FAST & EFFECTIVE, AS SAFE AS COFFEE
Compare to the active ingredient in
NoDoz®

CIRCLE K ™

maximum strength
no snooze™

Caffeine 200 mg,
Alertness Aid

[tablet image]

actual size

6 tablets (2 per pouch)

PRINCIPAL DISPLAY PANELPRINCIPAL DISPLAY PANEL

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
66715-583066715-5830-2, 66715-5830-3
66715-593066715-5930-2, 66715-5930-3
66715-553066715-5530-3

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 2 · 45 matching rows.

Name, UNII, Kind table
NameUNIIKind
CROSCARMELLOSE SODIUMM28OL1HH48IACT
SILICON DIOXIDEETJ7Z6XBU4IACT
D&C YELLOW NO. 1035SW5USQ3GIACT
DIBASIC CALCIUM PHOSPHATE DIHYDRATEO7TSZ97GEPIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
FD&C YELLOW NO. 6H77VEI93A8IACT
HYPROMELLOSE, UNSPECIFIED3NXW29V3WOIACT
MAGNESIUM STEARATE70097M6I30IACT
MICROCRYSTALLINE CELLULOSEOP1R32D61UIACT
POLYETHYLENE GLYCOL, UNSPECIFIED3WJQ0SDW1AIACT
POVIDONE, UNSPECIFIEDFZ989GH94EIACT
SODIUM STARCH GLYCOLATE TYPE A POTATO5856J3G2A2IACT
SUCROSEC151H8M554IACT
TITANIUM DIOXIDE15FIX9V2JPIACT
CAFFEINE3G6A5W338EACTIB
CROSCARMELLOSE SODIUMM28OL1HH48IACT
SILICON DIOXIDEETJ7Z6XBU4IACT
D&C YELLOW NO. 1035SW5USQ3GIACT
DIBASIC CALCIUM PHOSPHATE DIHYDRATEO7TSZ97GEPIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
FD&C YELLOW NO. 6H77VEI93A8IACT
HYPROMELLOSE, UNSPECIFIED3NXW29V3WOIACT
MAGNESIUM STEARATE70097M6I30IACT
MICROCRYSTALLINE CELLULOSEOP1R32D61UIACT
POLYETHYLENE GLYCOL, UNSPECIFIED3WJQ0SDW1AIACT
POVIDONE, UNSPECIFIEDFZ989GH94EIACT
SODIUM STARCH GLYCOLATE TYPE A POTATO5856J3G2A2IACT
SUCROSEC151H8M554IACT
TITANIUM DIOXIDE15FIX9V2JPIACT
CAFFEINE3G6A5W338EACTIB
CROSCARMELLOSE SODIUMM28OL1HH48IACT
SILICON DIOXIDEETJ7Z6XBU4IACT
D&C YELLOW NO. 1035SW5USQ3GIACT
DIBASIC CALCIUM PHOSPHATE DIHYDRATEO7TSZ97GEPIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
FD&C YELLOW NO. 6H77VEI93A8IACT
HYPROMELLOSE, UNSPECIFIED3NXW29V3WOIACT
MAGNESIUM STEARATE70097M6I30IACT
MICROCRYSTALLINE CELLULOSEOP1R32D61UIACT
POLYETHYLENE GLYCOL, UNSPECIFIED3WJQ0SDW1AIACT

Source Document#

Source XML

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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
e7119e49-e807-ad8b-e053-2995a90ab13474c871d1-b181-4e89-aecf-f864f5ce0ddc2022-08-25WarningsExact identifier
spl id: e7119e49-e807-ad8b-e053-2995a90ab134
spl set id: 74c871d1-b181-4e89-aecf-f864f5ce0ddc

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.