CONRX ALERT- caffeine tablet 
Eagle Distributors,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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ConRx™ Alert

Drug Facts

Active ingredient (in each caplet)

Caffeine 200 mg

Purpose

Alertness aid

Use

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 coffeube 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

in children under 12 years of age
as substitue 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

adults and children 12 years of age and over: take ½ to 1 caplet not more often than every 3 to 4 hours

Other information

store at room temperature

Inactive ingredients

benzoic acid, carnauba wax, corn starch, FD&C blue # 1, hypromellose, light mineral oil, microcrystalline cellulose, polysorbate 20, povidone, propylene glycol, simethicone emulsion, sorbitan monolaurate, stearic acid, sucrose,titanium dioxide.

Question or comments?

1-800-570-8650

PRINCIPAL DISPLAY PANEL - 50 Pouch Box

Compare to the Active Ingredients in
NoDoz

MAXIMUM STRENGTH
ConRx™

Alert
ALERTNESS AID

TO OPEN
PUSH IN TAB AND PULL OUT

Compare to the Active Ingredients in
NoDoz

50 Pouches of 2 Caplets Each

Principal Display Panel - 50 Pouch Box
CONRX ALERT 
caffeine tablet
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:68737-229
Route of Administration ORAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Caffeine (UNII: 3G6A5W338E) (Caffeine - UNII:3G6A5W338E) Caffeine 200 mg
Inactive Ingredients
Ingredient Name Strength
BENZOIC ACID (UNII: 8SKN0B0MIM)  
CARNAUBA WAX (UNII: R12CBM0EIZ)  
STARCH, CORN (UNII: O8232NY3SJ)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
HYPROMELLOSES (UNII: 3NXW29V3WO)  
LIGHT MINERAL OIL (UNII: N6K5787QVP)  
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
POLYSORBATE 20 (UNII: 7T1F30V5YH)  
POVIDONES (UNII: FZ989GH94E)  
POLYETHYLENE GLYCOL 6000 (UNII: 30IQX730WE)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
SORBITAN MONOLAURATE (UNII: 6W9PS8B71J)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
SUCROSE (UNII: C151H8M554)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
Product Characteristics
Color BLUE Score 2 pieces
Shape OVAL Size 11mm
Flavor Imprint Code CRX
Contains     
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:68737-229-13 50 in 1 BOX
1 2 in 1 POUCH
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC MONOGRAPH FINAL part340 02/15/2013
Labeler - Eagle Distributors,Inc. (929837425)

Revised: 2/2013
Document Id: c4310dbf-b2cf-4d72-a63a-11b34b148aef
Set id: b5479e47-9803-4ed7-bd9a-8eb39da20cea
Version: 1
Effective Time: 20130211
 
Eagle Distributors,Inc.