FDA.reportPublic FDA data

Eczemaforce

Manufacturer
BioActive Nutritional, Inc. | Apotheca Company
Effective date
2021-12-01
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:25:17

Label at a glance#

ProductEczemaforce
Active ingredientARCTIUM LAPPA ROOT, TRIFOLIUM PRATENSE FLOWER, PHYTOLACCA AMERICANA ROOT, CENTELLA ASIATICA, ARSENIC TRIOXIDE, GRAPHITE, DAPHNE MEZEREUM BARK
Label structure9 sections

Dosage and administration

10 drops orally, 3 times a day. Consult a physician for use in children under 12 years of age.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Lappa Major 3X, Trifolium Pratense 3X, Phytolacca Decandra 4X, Hydrocotyle Asiatica 6X, Arsenicum Album 12X, Graphites 12X, Mezereum 12X.

INDICATIONS:

OTC - PURPOSE SECTION

For temporary relief of skin irritations, urticaria and eczema.

WARNINGS:

WARNINGS SECTION

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.

Store in a cool, dry place.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

10 drops orally, 3 times a day. Consult a physician for use in children under 12 years of age.

INDICATIONS:

INDICATIONS & USAGE SECTION

For temporary relief of skin irritations, urticaria and eczema.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Demineralized Water, 25% Ethanol

QUESTIONS:

OTC - QUESTIONS SECTION

Distributed by:
BioActive Nutritional, Inc.
1803 N. Wickham Rd.
Melbourne, FL 32935
bioactivenutritional.com

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BIOActive Nutritional

ECZEMAFORCE

HOMEOPATHIC

1 FL OZ (30 ml)

EczemaforceEczemaforce

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43857-049743857-0497-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
ARCTIUM LAPPA ROOT597E9BI3Z3ACTIB
TRIFOLIUM PRATENSE FLOWER4JS0838828ACTIB
PHYTOLACCA AMERICANA ROOT11E6VI8VEGACTIB
CENTELLA ASIATICA7M867G6T1UACTIB
ARSENIC TRIOXIDES7V92P67HOACTIB
GRAPHITE4QQN74LH4OACTIB
DAPHNE MEZEREUM BARKX2N6E405GVACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT

Source Document#

Source XML · Source PDF

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
17c54366-8d22-410e-b6c6-a6bfe2cbf9d0cc82f93a-9925-4cd1-80af-4a9d4be2398e2021-12-01WarningsExact identifier
spl id: 17c54366-8d22-410e-b6c6-a6bfe2cbf9d0
spl set id: cc82f93a-9925-4cd1-80af-4a9d4be2398e

Reported adverse events (FAERS/openFDA)#

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