Scrofularoforce

Manufacturer
BioActive Nutritional, Inc. | Apotheca Company
Effective date
2021-12-01
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:25:10

Label at a glance#

ProductScrofularoforce
Active ingredientRUMEX CRISPUS ROOT, SCROPHULARIA NODOSA, ZANTHOXYLUM AMERICANUM BARK, SUS SCROFA LYMPH, BARIUM CARBONATE, BARIUM CHLORIDE DIHYDRATE, ATROPA BELLADONNA, OYSTER SHELL CALCIUM CARBONATE, CRUDE, CONIUM MACULATUM FLOWERING TOP, HELLEBORUS NIGER ROOT, IODINE, POTASSIUM PHOSPHATE, DIBASIC, LACHESIS MUTA VENOM, SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE, SILICON DIOXIDE, JUNIPERUS VIRGINIANA TWIG
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

Rumex Crispus 3X, Scrophularia Nodosa 3X, Xanthoxylum Fraxineum 3X, Lymph Node (Suis) 8X, Baryta Carbonica 12X, Baryta Muriatica 12X, Belladonna 12X, Calcarea Carbonica 12X, Conium Maculatum 12X, Helleborus Niger 12X, Iodium 12X, Kali Phosphoricum 12X, Lachesis Mutus 12X, Natrum Phosphoricum 12X, Silicea 12X, Juniperus Virginiana 16X.

INDICATIONS:

OTC - PURPOSE SECTION

For temporary relief of constricted feeling of the chest, palpitations with anxiety, purplish hue, burning, stinging pains, inflammation of connective tissues.

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 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 constricted feeling of the chest, palpitations with anxiety, purplish hue, burning, stinging pains, inflammation of connective tissues.

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

SCROFULAROFORCE

HOMEOPATHIC

1 FL OZ (30 ml)

ScrofularoforceScrofularoforce

Products#

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

DailyMed product names page 1 of 1 · 22 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43857-047943857-0479-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 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
545270a3-5985-4c09-befd-4c4665d58e4929050ced-bf79-4939-b093-4ad9005752df2021-12-01WarningsExact identifier
spl id: 545270a3-5985-4c09-befd-4c4665d58e49
spl set id: 29050ced-bf79-4939-b093-4ad9005752df

Reported adverse events (FAERS/openFDA)#

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