Label: NP THYROID- thyroid tablets tablet

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated August 10, 2025

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  • DOSAGE & ADMINISTRATION

    Take 1 tablet daily on an empty stomach or as directed.

  • WARNINGS

    Do not exceed recommended dose. Keep out of reach of children.

  • INACTIVE INGREDIENT

    Calcium stearate, dextrose, maltodextrin, mineral oil, modified wheat starch

  • INDICATIONS & USAGE

    Used as a thyroid hormone replacement for hypothyroidism.

  • PURPOSE

    Thyroid hormone replacement

  • ACTIVE INGREDIENT

    Thyroid 30 mg

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. In case of accidental overdose, contact a doctor or Poison Control Center immediately.

  • NDC 17224-502-30

    NDC 17224-502-30Package label for NP Thyroid 30 mg tablets (30 tablets per bottle). Contains product name, dosage strength, NDC 17224-502-30, manufacturer/repacker name, and usage instructions as printed on the label.

  • INGREDIENTS AND APPEARANCE
    NP THYROID 
    thyroid tablets tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:17224-502(NDC:42192-329)
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LIOTHYRONINE (UNII: 06LU7C9H1V) (LIOTHYRONINE - UNII:06LU7C9H1V) LIOTHYRONINE4.5 ug
    LEVOTHYROXINE (UNII: Q51BO43MG4) (LEVOTHYROXINE - UNII:Q51BO43MG4) LEVOTHYROXINE19 ug
    Inactive Ingredients
    Ingredient NameStrength
    ANHYDROUS DEXTROSE (UNII: 5SL0G7R0OK)  
    CALCIUM STEARATE (UNII: 776XM7047L)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    Product Characteristics
    Colorbrown (LIGHT BROWN,AS PER LABEL) Scoreno score
    ShapeROUND (STANDARD ROUND TABLET) Size5mm
    FlavorImprint Code AP;329
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:17224-502-3030 in 1 BOTTLE; Type 0: Not a Combination Product08/01/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other08/01/2025
    Labeler - Calvin Scott & Co Inc. (073404626)
    Establishment
    NameAddressID/FEIBusiness Operations
    Calvin Scott & Co Inc.073404626repack(17224-502)