Label: PAMPRIN BLOAT- pamabrom tablet, film coated

  • NDC Code(s): 71687-3009-1
  • Packager: Focus Consumer Healthcare, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 31, 2025

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  • Active ingredient (in each caplet)

    Pamabrom 50 mg

  • Purpose



    Diuretic

  • Uses

    For the temporary relief of

    • bloating
    • water-weight gain
    • swelling
    • full feeling

    associated with the premenstrual and menstrual periods.

  • Warnings


  • Do not use

    Do not use if you have ever had an allergic reaction to this product or any of its ingredients.

  • PREGNANCY OR BREAST FEEDING

    If pregnant or breastfeeding, ask a health professional before use.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

  • Directions

    • do not take more than the recommended dose
    • adults and children 12 years and older:
    • take 1 caplet with water
    • repeated every 6 hours, as needed
    • do not exceed 4 caplets per day
    • children under 12 years: consult a doctor
  • Other information

    Each caplet contains: 170 mg of Calcium

  • Inactive ingredients

    calcium sulfate dihydrate, croscarmellose sodium, dibasic calcium phosphate dihydrate, FDC Blue #1 lake, hypromellose, magnesium stearate, mineral oil, polyethylene glycol, potassium gluconate, riboflavin, sodium lauryl sulfate, stearic acid, talc, titanium dioxide

  • PRINCIPAL DISPLAY PANEL

    PDP

  • INGREDIENTS AND APPEARANCE
    PAMPRIN  BLOAT
    pamabrom tablet, film coated
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71687-3009
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PAMABROM (UNII: UA8U0KJM72) (BROMOTHEOPHYLLINE - UNII:FZG87K1MQ6) PAMABROM50 mg
    Inactive Ingredients
    Ingredient NameStrength
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP)  
    FD&C BLUE NO. 1 ALUMINUM LAKE (UNII: J9EQA3S2JM)  
    HYPROMELLOSES (UNII: 3NXW29V3WO)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    LIGHT MINERAL OIL (UNII: N6K5787QVP)  
    POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
    POTASSIUM GLUCONATE (UNII: 12H3K5QKN9)  
    CALCIUM SULFATE DIHYDRATE (UNII: 4846Q921YM)  
    RIBOFLAVIN (UNII: TLM2976OFR)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    TALC (UNII: 7SEV7J4R1U)  
    Product Characteristics
    ColorblueScoreno score
    ShapeOVALSize15mm
    FlavorImprint Code P
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71687-3009-11 in 1 CARTON12/31/2025
    130 in 1 BOTTLE; Type 0: Not a Combination Product
    Image of Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02712/31/2025
    Labeler - Focus Consumer Healthcare, LLC (080743737)
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