Label: KALI PHOSPHORICUM spray

  • Category: HUMAN OTC DRUG LABEL

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 May 25, 2023

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

  • ACTIVE INGREDIENT:

    (in each drop) Kali Phosphoricum 6X 100%.

  • PURPOSE:

    Kali Phosphoricum - nervousness*

  • USES:

    May temporarily relieve stress, irritability, mental exhaustion, sleeplessness, low mood, and nerve-related aches.*

    *Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

  • WARNINGS:

    For oral use only.

    If pregnant or breast-feeding, ask a health care professional before use.

    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:

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

  • DIRECTIONS:

    • Adults: 2 sprays 3 times a day in mouth or half a cup of water

    • Children under 12: 1 spray as above

    •  Consult a physician for use in children under 12 years of age.

    Store in a cool, dry place.

  • INACTIVE INGREDIENTS:

    Demineralized water, 20% organic ethanol 

  • QUESTIONS:

    Dist. by Ratis, LLC

    1201 N Orange St,

    Ste 7594

    Wilmington, DE 19801

    www.HomeopathyStore.com

    (888) 405-7551

  • PACKAGE LABEL DISPLAY:

    SCHUESSLER CELL SALTS

    LACTOSE FREE

    ANNA

    KARE

    Kali

    Phosphoricum

    HOMEOPATHIC ORAL SPRAY

    1 FL. OZ (30ML)

    Kali Phosphoricum

  • INGREDIENTS AND APPEARANCE
    KALI PHOSPHORICUM 
    kali phosphoricum spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71753-8006
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DIBASIC POTASSIUM PHOSPHATE (UNII: CI71S98N1Z) (PHOSPHATE ION - UNII:NK08V8K8HR) DIBASIC POTASSIUM PHOSPHATE6 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71753-8006-130 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product09/30/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic09/30/2020
    Labeler - Ratis, LLC (964594324)