Label: THYMULINE liquid

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

DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

Drug Label Information

Updated March 8, 2022

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  • ACTIVE INGREDIENT:

    Thymuline 9C

  • INDICATIONS:

    Immune system support.**

    **These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

  • WARNINGS:

    For oral use only.

    If pregnant or breast-feeding, or if symptoms persist or worsen or worsen, ask a health care professional.

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

    Do not use if tamper evident seal is broken or missing.

  • KEEP OUT OF REACH OF CHILDREN:

    Keep out of reach of children. In case of overdose, contact physician or Poison Control Center right away.

  • DIRECTIONS:

    4-5 sprays under tongue or in a small glass of water once a week or as needed. Children 2-12: 2-3 sprays as above. For children 12 and under, consult a doctor. Store in a cool, dry place.

  • INDICATIONS:

    Immune system support.**

    **These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

  • INACTIVE INGREDIENTS:

    Demineralized Water, Glycerin, Organic Ethanol 10%

  • QUESTIONS:

    Questions? Comments?

    Visit HomeopathyStore.com or call (888) 405-7551.

    Distributed by: Ratis, LLC,

    211 E Lombard St,

    STE 303, Baltimore, MD 21202

  • PACKAGE LABEL DISPLAY:

    NDC 71753-1152-1

    Anna's

    REMEDIES

    Thymuline

    IMMUNE SYSTEM SUPPORT**

    HOMEOPATHIC ORAL SPRAY

    1 FL. OZ (30ML)

    Thymuline

  • INGREDIENTS AND APPEARANCE
    THYMULINE 
    thymuline liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71753-1152
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    NONATHYMULIN (UNII: 9H198D04WL) (NONATHYMULIN - UNII:9H198D04WL) NONATHYMULIN9 [hp_C]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71753-1152-130 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product09/06/201812/01/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic09/06/201812/01/2025
    Labeler - Ratis, LLC (964594324)
    Registrant - Apotheca Company (844330915)
    Establishment
    NameAddressID/FEIBusiness Operations
    Apotheca Company844330915manufacture(71753-1152) , api manufacture(71753-1152) , label(71753-1152) , pack(71753-1152)
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