Label: CONRX ALERT- caffeine tablet
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Contains inactivated NDC Code(s)
NDC Code(s): 68737-229-13 - Packager: Eagle Distributors,Inc.
- Category: HUMAN OTC DRUG LABEL
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.
Drug Label Information
Updated February 11, 2013
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient (in each caplet)
- Purpose
- Use
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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.
- Directions
- Other information
- Inactive ingredients
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- PRINCIPAL DISPLAY PANEL - 50 Pouch Box
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INGREDIENTS AND APPEARANCE
CONRX ALERT
caffeine tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68737-229 Route of Administration ORAL 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)