CONRX ALERT- caffeine tablet

United States - English - NLM (National Library of Medicine)

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Active ingredient:
Caffeine (UNII: 3G6A5W338E) (Caffeine - UNII:3G6A5W338E)
Available from:
Eagle Distributors,Inc.
INN (International Name):
Caffeine
Composition:
Caffeine 200 mg
Administration route:
ORAL
Prescription type:
OTC DRUG
Therapeutic indications:
Alertness aid
Authorization status:
OTC monograph final
Authorization number:
68737-229-13

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

Purpos e

Alertness aid

Us e

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

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

helps restore mental alertness or wakefulness when experiencing fatigue or drowsiness

in children under 12 years of age

as substitue for sleep

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

hours

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

CONRX ALERT

caffeine tablet

Product Information

Product T ype

HUMAN OTC DRUG

Ite m Code (Source )

NDC:6 8 737-229

Route of Administration

ORAL

Active Ingredient/Active Moiety

Ingredient Name

Basis of Strength

Stre ng th

Ca ffeine (UNII: 3G6 A5W338 E) (Caffeine - UNII:3G6 A5W338 E)

Ca ffe ine

20 0 mg

Inactive Ingredients

Ingredient Name

Stre ng th

BENZO IC ACID (UNII: 8 SKN0 B0 MIM)

CARNAUBA WAX (UNII: R12CBM0 EIZ)

STARCH, CO RN (UNII: O8 232NY3SJ)

FD&C BLUE NO . 1 (UNII: H3R47K3TBD)

HYPRO MELLO SES (UNII: 3NXW29 V3WO)

LIGHT MINERAL O IL (UNII: N6 K578 7QVP)

CELLULO SE, MICRO CRYSTALLINE (UNII: OP1R32D6 1U)

PO LYSO RBATE 2 0 (UNII: 7T1F30 V5YH)

PO VIDO NES (UNII: FZ9 8 9 GH9 4E)

PO LYETHYLENE GLYCO L 6 0 0 0 (UNII: 30 IQX730 WE)

Eagle Distributors,Inc.

DIMETHICO NE (UNII: 9 2RU3N3Y1O)

SO RBITAN MO NO LAURATE (UNII: 6 W9 PS8 B71J)

STEARIC ACID (UNII: 4ELV7Z6 5AP)

SUCRO SE (UNII: C151H8 M554)

TITANIUM DIO XIDE (UNII: 15FIX9 V2JP)

Product Characteristics

Color

BLUE

S core

2 pieces

S hap e

OVAL

S iz e

11mm

Flavor

Imprint Code

Contains

Packag ing

#

Item Code

Package Description

Marketing Start Date

Marketing End Date

1

NDC:6 8 737-229 -13

50 in 1 BOX

1

2 in 1 POUCH

Marketing Information

Marke ting Cate gory

Application Numbe r or Monograph Citation

Marke ting Start Date

Marke ting End Date

OTC MONOGRAPH FINAL

pa rt340

0 2/15/20 13

Labeler -

Eagle Distributors,Inc. (929837425)

Revised: 2/2013

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