Label: DIUREX ULTRA- caffeine tablet, film coated
- NDC Code(s): 52389-155-02, 52389-155-80, 52389-155-90
- Packager: Kobayashi Healthcare International, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated April 14, 2025
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
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Active ingredient (in each pill)Caffeine Anhydrous, 100 mg
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PurposeDiuretic
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UsesFor the relief of: temporary water retention - bloating - swelling - full feeling - fatigue - associated with the pre-menstrual and menstrual periods
- Warnings
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Ask a doctor before use iftaking any other medications - under 18 years of age. Do not give to children under 12 years of age.
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WHEN USINGWhen using this product, limit the use of caffeine-containing medications, foods or beverages because too much caffeine may cause: nervousness - irritability - sleeplessness - occasional ...
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STOP USEStop use and ask a doctor if symptoms last for more than ten consecutive days.
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PREGNANCY OR BREAST FEEDINGIf pregnant or breastfeeding, ask a health professional before use.
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KEEP OUT OF REACH OF CHILDRENKeep out of the reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
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DirectionsRead all package directions and warnings before use. Use only as directed. Adults: One (1) pill (100 mg) or two (2) pills (200 mg maximum strength) every 3 to 4 hours wile symptoms persist, not ...
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Other informationCalcium content: 30 mg/pill - Identification: Light green colored, round pill bearing the identifying mark "ALVA". **Contents sealed: Contents packaged in a bottle with a safety seal under the ...
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Inactive ingredientsAcacia, calcium carbonate, croscarmellose sodium, D&C Yellow No. 10 Lake, ethyl vanillin, FD&C Blue No. 1 Lake, FD&C Blue No. 2 Lake, hypromellose, lactose, magnesium silicate, magnesium ...
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QUESTIONSQuestions? 1-800-792-2582
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PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCEProduct Information