NODOZ ALERTNESS AID  MAXIMUM STRENGTH- caffeine tablet, film coated 
Lil' Drug Store Products, Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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NoDoz® Alertness Aid

Maximum Strength

Drug Facts

Active ingredient (in each caplet)

Caffeine 200 mg

Purpose

Alertness aid

Use

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 heartbeat.

Do not use

  • in children under 12 years of age
  • as 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.

Directions

Other information

Inactive ingredients

carnauba wax, corn starch, FD&C blue #1, hypromellose, microcrystalline cellulose, povidone K30, propylene glycol, stearic acid, sucrose, titanium dioxide

Questions or comments?

call toll-free 1-877-507-6516 (M-F 8AM-4:30PM CST) or www.nodoz.com

PRINCIPAL DISPLAY PANEL - 200 mg Caplet Pouch Carton

Max Strength • Fast Acting

NoDoz®

Alertness Aid

200 mg CAFFEINE EACH

4
CAPLETS
2 POUCHES, 2 CAPLETS PER POUCH

Lil'
Drug Store ®

PRINCIPAL DISPLAY PANEL - 200 mg Caplet Pouch Carton
NODOZ ALERTNESS AID   MAXIMUM STRENGTH
caffeine tablet, film coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66715-9799
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CAFFEINE (UNII: 3G6A5W338E) (CAFFEINE - UNII:3G6A5W338E) CAFFEINE200 mg
Inactive Ingredients
Ingredient NameStrength
CARNAUBA WAX (UNII: R12CBM0EIZ)  
STARCH, CORN (UNII: O8232NY3SJ)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
SUCROSE (UNII: C151H8M554)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
Product Characteristics
ColorwhiteScore2 pieces
ShapeOVAL (Caplet) Size15mm
FlavorImprint Code NoDoz
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:66715-9799-42 in 1 CARTON12/07/2017
110 in 1 BLISTER PACK; Type 0: Not a Combination Product
2NDC:66715-9799-33 in 1 CARTON12/07/2017
22 in 1 POUCH; Type 0: Not a Combination Product
3NDC:66715-9799-61 in 1 CARTON12/07/2017
360 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
4NDC:66715-9799-22 in 1 CARTON06/01/2018
42 in 1 POUCH; Type 0: Not a Combination Product
5NDC:66715-9799-010 in 1 VIAL, PLASTIC; Type 0: Not a Combination Product04/01/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34012/07/2017
Labeler - Lil' Drug Store Products, Inc. (093103646)

Revised: 7/2021
Document Id: c72b4091-8ab2-1e7b-e053-2a95a90a517c
Set id: 54d47b7a-66a1-4f86-b478-f2f8737cd030
Version: 5
Effective Time: 20210715
 
Lil' Drug Store Products, Inc.