Psoriaforce

Manufacturer
BioActive Nutritional, Inc. | Apotheca Company
Effective date
2024-09-27
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 20:54:02

Label at a glance#

ProductPsoriaforce
Active ingredientBAPTISIA TINCTORIA ROOT, BERBERIS VULGARIS ROOT BARK, ECHINACEA ANGUSTIFOLIA WHOLE, GLYCYRRHIZA GLABRA, ARCTIUM LAPPA ROOT, FRANGULA ALNUS BARK, FRANGULA PURSHIANA BARK, TRIFOLIUM PRATENSE FLOWER, ZANTHOXYLUM AMERICANUM BARK, PHYTOLACCA AMERICANA ROOT, GOLDENSEAL, ARSENIC TRIIODIDE, OYSTER SHELL CALCIUM CARBONATE, CRUDE, CLEMATIS RECTA FLOWERING TOP, GRAPHITE, POTASSIUM CHLORIDE, POTASSIUM SULFATE, DAPHNE MEZEREUM BARK, KEROSENE, SEPIA OFFICINALIS JUICE
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

Baptisia Tinctoria 3X, Berberis Vulgaris 3X, Echinacea (Angustifolia) 3X, Glycyrrhiza Glabra 3X, Lappa Major 3X, Rhamnus Frangula 3X, Rhamnus Purshiana 3X, Trifolium Pratense 3X, Xanthoxylum Fraxineum 3X, Phytolacca Decandra 4X, Hydrastis Canadensis 5X, Arsenicum Iodatum 12X, Calcarea Carbonica 12X, Clematis Erecta 12X, Graphites 12X, Kali Muriaticum 12X, Kali Sulphuricum 12X, Mezereum 12X, Petroleum 12X, Sepia 12X.

INDICATIONS:

OTC - PURPOSE SECTION

For temporary relief of unhealthy irritated or broken skin, itching, burning, swelling of skin, dry rough, scaly skin and eruptions on scalp and bends of joints with itching.

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 attention 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 attention 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 unhealthy irritated or broken skin, itching, burning, swelling of skin, dry rough, scaly skin and eruptions on scalp and bends of joints with itching.

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

PSORIAFORCE

HOMEOPATHIC

1 FL OZ (30 ml)

PsoriaforcePsoriaforce

Products#

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

DailyMed product names page 1 of 1 · 27 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43857-046943857-0469-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 22 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
4aceef88-d211-451c-852a-ed9ee31bc39031c24882-cb44-4fa7-a584-9f4945215a432024-09-27WarningsExact identifier
spl id: 4aceef88-d211-451c-852a-ed9ee31bc390
spl set id: 31c24882-cb44-4fa7-a584-9f4945215a43

Reported adverse events (FAERS/openFDA)#

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