ECZEMA CONTROL- centella asiatica, iris versicolor root, arctium lappa root, sodium chloride, ruta graveolens flowering top, silicon dioxide, taraxacum officinale, and thuja occidentalis root solution/ drops

Eczema Control by

Drug Labeling and Warnings

Eczema Control by is a Homeopathic medication manufactured, distributed, or labeled by Forces of Nature. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

  • Also Contains

    Sesame Oil1, Lavandin Oil1, Palmarosa Oil1, Pine Oil1, Rosemary Oil1, Niaouli Oil1, German Chamomile Oil1

  • Indications

    For the temporary relief of itching associated with minor skin irritations and rashes which may be due to Eczema.

  • Directions

    Apply to affected area by gently rubbing into the skin 3 or 4 times daily. For children under 2 years of age, consult a doctor before use.

  • Warnings

    Some individuals may be sensitive to essential oils. Begin with a small drop to determine if the product causes any increased redness or irritation and discontinue use if it irritates your skin.

    For external use only. If accidental ingestion of more than several drops, and adverse reaction occurs, get medical help or contact a Poison Control Center. Do not apply to the eyes. If you are pregnant or breast -feeding, ask a health professional before use. Not for use on children under the age of 3.

    Keep all medicines out of the reach of children.

    Stop use and consult a doctor if condition worsens, or consult a doctor if symptoms show no improvement after 7 days.

  • SPL UNCLASSIFIED SECTION

    Manufactured & Distributed by
    FORCES OF NATURE®
    21787 8th St East #3A Sonoma, CA 95476 USA

  • PRINCIPAL DISPLAY PANEL - 5 ml Bottle Box

    ORGANIC

    NDC #51393-5622-5

    FORCES OF NATURE®

    CERTIFIED ORGANIC MEDICINE

    Eczema

    CONTROL

    Topical Eczema Medicine

    Lappa Arctium

    .17 OZ/5 ml

    PRINCIPAL DISPLAY PANEL - 5 ml Bottle Box
  • INGREDIENTS AND APPEARANCE
    ECZEMA CONTROL 
    centella asiatica, iris versicolor root, arctium lappa root, sodium chloride, ruta graveolens flowering top, silicon dioxide, taraxacum officinale, and thuja occidentalis root solution/ drops
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 51393-5622
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Centella Asiatica (UNII: 7M867G6T1U) (Centella Asiatica - UNII:7M867G6T1U) Centella Asiatica12 [hp_C]  in 100 mL
    Iris Versicolor Root (UNII: X43D4L3DQC) (Iris Versicolor Root - UNII:X43D4L3DQC) Iris Versicolor Root12 [hp_C]  in 100 mL
    Arctium Lappa Root (UNII: 597E9BI3Z3) (Arctium Lappa Root - UNII:597E9BI3Z3) Arctium Lappa Root12 [hp_C]  in 100 mL
    Sodium Chloride (UNII: 451W47IQ8X) (Chloride Ion - UNII:Q32ZN48698, Sodium Cation - UNII:LYR4M0NH37) Sodium Chloride12 [hp_X]  in 100 mL
    Ruta Graveolens Flowering Top (UNII: N94C2U587S) (Ruta Graveolens Flowering Top - UNII:N94C2U587S) Ruta Graveolens Flowering Top12 [hp_C]  in 100 mL
    Silicon Dioxide (UNII: ETJ7Z6XBU4) (Silicon Dioxide - UNII:ETJ7Z6XBU4) Silicon Dioxide6 [hp_X]  in 100 mL
    Taraxacum Officinale (UNII: 39981FM375) (Taraxacum Officinale - UNII:39981FM375) Taraxacum Officinale6 [hp_C]  in 100 mL
    Thuja Occidentalis Root (UNII: 12958C0BR3) (Thuja Occidentalis Root - UNII:12958C0BR3) Thuja Occidentalis Root8 [hp_X]  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    Pine Needle Oil (Pinus Sylvestris) (UNII: 5EXL5H740Y)  
    Rosemary Oil (UNII: 8LGU7VM393)  
    Lavandin Oil (UNII: 9RES347CKG)  
    Niaouli Oil (UNII: D50IC2T8FU)  
    Palmarosa Oil (UNII: 0J3G3O53ST)  
    Matricaria Chamomilla Flowering Top Oil (UNII: SA8AR2W4ER)  
    Sesame Oil (UNII: QX10HYY4QV)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 51393-5622-111 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product12/01/2011
    2NDC: 51393-5622-233 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product12/01/2011
    3NDC: 51393-5622-55 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product07/01/2016
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    UNAPPROVED HOMEOPATHIC12/01/2011
    Labeler - Forces of Nature (050169130)

  • Trademark Results [Eczema Control]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    ECZEMA CONTROL
    ECZEMA CONTROL
    86682216 not registered Dead/Abandoned
    Blistex Inc.
    2015-07-02

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.