Label: CANNABIS SATIVA 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 22, 2023

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  • ACTIVE INGREDIENT

    CANNABIS SATIVA 1X

    (Cannabidiol) 100mg per mL Delta 9 THC < 0.3%

  • PURPOSE

    LESSENS PAIN, IMPROVES APPETITE, AND CAUSES SLEEP

  • WARNING:

    "The FDA has not determined that this product is safe, effective and not misbranded for its intended use."

  • INDICATIONS & USAGE

    To be used according to standard homeopathic indications for self-limiting conditions such as those indicated above or as directed by a physician.

  • KEEP OUT OF REACH OF CHILDREN

    Keep this and all medication out of reach of children.

  • Warning:

    Use only if cap and seal are unbroken. If symptoms persist for more than 3 days or worsen, discontinue (STOP) use and consult your physician. As with any drug, if you are pregnant or nursing (breast-feeding) a baby, seek the advise of a health professional before using this product. Store tightly closed in a cool area.

  • Directions:

    Take 1mL by mouth or as directed by a physician.

  • Other information:

    Contains approx. 30 doses.

  • Inactive Ingredients:

    MCT Oil, Alcohol, and Strawberry Flavoring. Free from yeast, wheat, corn, and soy.

  • Questions or comments

    (877) REM4YOU Fax (909) 594-4205 Pomona, CA 91768. USA

  • PRINCIPAL DISPLAY PANEL

    Sample Label

  • INGREDIENTS AND APPEARANCE
    CANNABIS SATIVA 
    cannabis sativa liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10191-6374
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CANNABIS SATIVA FLOWERING TOP (UNII: 8X454SZ22D) (CANNABIDIOL - UNII:19GBJ60SN5) CANNABIS SATIVA FLOWERING TOP1 [hp_X]  in 30 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:10191-6374-130 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product03/22/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic03/22/2023
    Labeler - Remedy Makers (018543582)
    Registrant - Remedy Makers (018543582)
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