Eczema Control

Manufacturer
Forces of Nature
Effective date
2010-08-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:02:32

Label at a glance#

ProductEczema Control
Active ingredientChamomile, Graphite, Hypericum Perforatum
Label structure12 sections

Dosage and administration

Apply product directly to affected area and rub gently into the skin. Repeat 3 times per day. It may also help to apply a few drops to the soles of each foot 2-3 times per day, as well.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Indications

INDICATIONS & USAGE SECTION

For the treatment of eczema

OTC - ACTIVE INGREDIENT SECTION

OTC - PURPOSE SECTION

Homeopathic Active Ingredients*
Equal parts of: Purpose
Chamomilla 6X HPUSTo improve unhealthy skin
Graphites 6X HPUSRelief from eczema, dry rough irritated skin
Hypericum 6X HPUS For relief of eczema of face and hands

* The letters 'HPUS' indicate that the components in this product are officially monographed in the Homœopathic Pharmacopœia of the United States.

Also Contains

INACTIVE INGREDIENT SECTION

Certified Organic Oils of: Carrot Seed, Helichrysum, Lavandin Super, Melaleuca Quinquenervia Leaf Oil, Roman Chamomile, Rosemary, Sesame Seed, and Tea Tree, Rosa Moschata

Directions

DOSAGE & ADMINISTRATION SECTION

Apply product directly to affected area and rub gently into the skin. Repeat 3 times per day. It may also help to apply a few drops to the soles of each foot 2-3 times per day, as well.

Warnings

WARNINGS SECTION

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.

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

OTC - WHEN USING SECTION

For external use only. If accidental ingestion more than several drops, and adverse reaction occurs, get medical help or contact a Poison Control Center. Do not apply to the eyes; in the event of contact, flush with water and seek advice from medical personnel.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Not to be used with children under 2 years of age. Keep all medicines out of the reach of children.

OTC - STOP USE SECTION

Stop use and ask a doctor if condition worsens, symptoms last more than 7 days, or clear up and occur again within a few days.

SPL UNCLASSIFIED SECTION

Manufactured by:
Forces of Nature, Inc.
55 Galli Drive, Suite C
Novato, CA 94949 USA
www.fonworld.org

Product questions?

OTC - QUESTIONS SECTION

877-975-3797

SPL UNCLASSIFIED SECTION

NDC#: 51393-6222-1 (11ml) // 51393-6222-2 (33ml)

PRINCIPAL DISPLAY PANEL - 11 ml Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Forces of Nature

Eczema Control

0.38 fl. oz. / 11 ml

Principal Display Panel - 11 ml Bottle Label
Principal Display Panel - 11 ml Bottle Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51393-6222-12019-10-21C16284748780-1956f9ecf-c5b8-621f-e053-dbdaa90a74adEczema Control
51393-6222-22019-10-21C16284748780-1956f9ecf-c5b8-621f-e053-dbdaa90a74adEczema Control

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51393-6222-1Eczema Control11 mL in 1 BOTTLE, DISPENSINGSOLUTION/ DROPS111
51393-6222-2Eczema Control33 mL in 1 BOTTLE, DISPENSINGSOLUTION/ DROPS331

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51393-6222ECZEMA CONTROL (CHAMOMILE, GRAPHITE, AND HYPERICUM PERFORATUM) SOLUTION/ DROPS [FORCES OF NATURE]1Legacy NDC, 2 package rows20100903_4c95202e-f67e-4647-87b3-3df92fa0776d.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ChamomileACTIVE INGREDIENTFGL3685T2X1
GraphiteACTIVE INGREDIENT4QQN74LH4O1
Hypericum PerforatumACTIVE INGREDIENTXK4IUX8MNB1
ChamomileACTIVE MOIETYFGL3685T2X1
GraphiteACTIVE MOIETY4QQN74LH4O1
Hypericum PerforatumACTIVE MOIETYXK4IUX8MNB1
Tea Tree OilINACTIVE INGREDIENTVIF565UC2G1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51393-622251393-6222-1, 51393-6222-2

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
deb4d864-325a-4cfa-8830-ef36c54ff9ca4c95202e-f67e-4647-87b3-3df92fa0776d2010-08-24WarningsExact identifier
spl id: deb4d864-325a-4cfa-8830-ef36c54ff9ca
spl set id: 4c95202e-f67e-4647-87b3-3df92fa0776d

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.