Label: SOLCURE WATER BALM- illite stick

  • 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 February 1, 2023

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

View All Sections
  • ACTIVE INGREDIENT

    illite

  • INACTIVE INGREDIENT

    Glycerin
    Dipropylene Glycol
    Chamaecyparis Obtusa Water
    Water
    Palmitic acid
    Stearic Acid
    Ectoin
    Vincetoxicum Atratum Extract
    Butylene Glycol
    Fucus Vesiculosus Extract
    Prunella Vulgaris Extract
    Sodium Hydroxide

  • PURPOSE

    skin protentant

  • KEEP OUT OF REACH OF CHILDREN

    keep out or reach of the children

  • INDICATIONS & USAGE

    Apply an appropriate amount to the skin

  • WARNINGS

    This product is for exeternal use only. Do not use for internal use
    Storage and handling precautions
    If possible, avoid direct sunlight and store in cool and area of low humidity in order to maintain the quality of the product and avoid misuse
    Avoid placing the product near fire and store out in reach of children

    - consult a physician in case of abnormal symptoms, such as red spots, swelling or itching, or side effects in the areas of application due to direct light during or after using the product

    - do not use on wounded area

  • DOSAGE & ADMINISTRATION

    for external use only

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    SOLCURE WATER BALM 
    illite stick
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83235-0003
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LEDIKITE (UNII: D7BC5B0F46) (LEDIKITE - UNII:D7BC5B0F46) LEDIKITE0.01 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83235-0003-112 g in 1 PACKAGE; Type 0: Not a Combination Product02/01/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other02/01/2023
    Labeler - Erae Natural Life (695930484)
    Registrant - Erae Natural Life (695930484)
    Establishment
    NameAddressID/FEIBusiness Operations
    Erae Natural Life695930484manufacture(83235-0003)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!