VAX

Manufacturer
BioActive Nutritional, Inc. | Apotheca Company
Effective date
2023-08-25
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:26:51

Label at a glance#

ProductVAX
Active ingredientBAPTISIA TINCTORIA, ECHINACEA ANGUSTIFOLIA, GOLDENSEAL, TABEBUIA IMPETIGINOSA BARK, TRIFOLIUM PRATENSE FLOWER, ARNICA MONTANA, CALENDULA OFFICINALIS FLOWERING TOP, CHELIDONIUM MAJUS, VERONICASTRUM VIRGINICUM ROOT, LIGUSTICUM PORTERI ROOT, LOMATIUM DISSECTUM ROOT, MYRRH, NASTURTIUM OFFICINALE, PHYTOLACCA AMERICANA ROOT, TARAXACUM OFFICINALE, FENUGREEK SEED, URTICA DIOICA, ASTRAGALUS PROPINQUUS ROOT, PROPOLIS WAX, SUS SCROFA ADRENAL GLAND, SUS SCROFA THYMUS, ARSENIC TRIOXIDE, ATROPA BELLADONNA, CHAMOMILE, LYCOPODIUM CLAVATUM SPORE, TOXICODENDRON PUBESCENS LEAF, SILICON DIOXIDE, THUJA OCCIDENTALIS LEAFY TWIG, ANTIMONY TRISULFIDE, BORDETELLA PERTUSSIS, TETANUS TOXIN, THIMEROSAL
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, Echinacea (Angustifolia) 3X, Hydrastis Canadensis 3X, Tabebuia Impetiginosa 3X, Trifolium Pratense 3X, Arnica Montana 4X, Calendula Officinalis 4X, Chelidonium Majus 4X, Leptandra Virginica 4X, Ligusticum Porteri 4X, Lomatium Dissectum 4X, Myrrha 4X, Nasturtium Aquaticum 4X, Phytolacca Decandra 4X, Taraxacum Officinale 4X, Trigonella Foenum-Graecum 4X, Urtica Dioica 4X, Astragalus Membranaceus 6X, Propolis 6X, Glandula Suprarenalis Suis 8X, Thymus (Suis) 8X, Arsenicum Album 12X, Belladonna 12X, Chamomilla 12X, Lycopodium Clavatum 12X, Rhus Tox 12X, Silicea 30X, Thuja Occidentalis 30X, Antimonium Crudum 30X, 200X, Pertussinum 30C, Tetanus Toxin 30X, Thimerosal 30C.

INDICATIONS:

OTC - PURPOSE SECTION

For temporary relief of skin irritation, dry cough, eczema, and fever.

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 skin irritation, dry cough, eczema, and fever.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Demineralized Water, 25% Ethanol.

QUESTIONS:

OTC - QUESTIONS SECTION

Distributed by:

BIOACTIVE NUTRITIONAL

Melbourne, FL 32935

For Nutritional Information write:

BioActive Nutritional, Inc.

1803 N. Wickham Rd.

Melbourne, FL 32935

PAKCAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BioActive Homeopathic
VAX
1 FL OZ (30 ml)

VAXVAX

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
43857-0386-12023-08-25C16284748780-19d75b9d0-d75c-f424-e053-dadaa90a57ceDrug Facts:
43857-0386-12020-01-31C16284748780-19d75b9d0-d75c-f424-e053-dadaa90a57ceDrug Facts:

Products#

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

DailyMed product names page 1 of 1 · 39 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43857-038643857-0386-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 34 matching rows.

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
1971c48d-2d77-47e7-a63f-50340d0b5d619efc6013-5535-4010-be95-b4aa025b36092023-08-25WarningsExact identifier
spl id: 1971c48d-2d77-47e7-a63f-50340d0b5d61
spl set id: 9efc6013-5535-4010-be95-b4aa025b3609

Reported adverse events (FAERS/openFDA)#

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