Label: PINRID- pyrantel pamoate tablet

  • NDC Code(s): 73581-107-12, 73581-107-24
  • Packager: YYBA CORP
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 3, 2024

If you are a consumer or patient please visit this version.

  • ACTIVE INGREDIENT

    PYRANTEL PAMOATE 720.5 MG

  • PURPOSE

    PINROOM TREATMENT

  • USE

    FOR THE TREATMENT OF PINWORMS

  • WARNINGS

    IF ANY OF THESE CONDITIONS PERSIST, CONSULT A DOCTOR

    • DIZZINESS
    • DIARHEA
    • ABDOMINAL CRAMPS
    • VOMITING
    • NAUSEA
    • HEADACHE

    IF PREGNANT OR IF YOU HAVE LIVER DISEASE, ASK A DOCTOR BEFORE USE. CONSULT YOUR DOCTOR IF AN ALLERGIC REACTION OCCURS.

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN. IN CASE OF ACCIDENTAL OVERDOSE, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

  • DIRECTIONS FOR USE

    Directions_Pinrid_12ct

  • OTHER INFORMATION

    • PHENYLKETONURICS: CONTAIN PHENYLALANINE 11.8 MG PER TABLET
    • READ PACKAGE INSERT CAREFULLY BEFORE USING
    • IF SIGNS OF PINWORMS PERSIST, SEE A DOCTOR
    • STORE AT 15° - 30°c (59° - 86°f)
  • INACTIVE INGREDIENTS

    aspartame powder, citric acid, colloidal silicon dioxide, croscarmellose sodium, dextrose, FD&C yellow, magnesium stearate, maltodextrin, sorbitol, stearic acid, orange fl avor.

  • QUESTIONS OR COMMENTS?

    CALL TOLL FREE 1-866-933-6337

  • PRINCIPAL DISPLAY PANEL

    01b LBL_Pinrid_12ct

    01b LBL_Pinrid_24ct

  • INGREDIENTS AND APPEARANCE
    PINRID 
    pyrantel pamoate tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73581-107
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PYRANTEL PAMOATE (UNII: 81BK194Z5M) (PYRANTEL - UNII:4QIH0N49E7) PYRANTEL250 mg
    Inactive Ingredients
    Ingredient NameStrength
    ASPARTAME (UNII: Z0H242BBR1)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    DEXTROSE (UNII: IY9XDZ35W2)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    SORBITOL (UNII: 506T60A25R)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeROUNDSize11mm
    FlavorImprint Code WM1
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73581-107-1212 in 1 BOTTLE; Type 0: Not a Combination Product04/02/2021
    2NDC:73581-107-2424 in 1 BOTTLE; Type 0: Not a Combination Product04/02/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM03104/02/2021
    Labeler - YYBA CORP (006339772)