Bio Tonsilla Phase

Manufacturer
Deseret Biologicals, Inc. | Apotheca Company
Effective date
2021-09-21
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:35:08

Label at a glance#

ProductBio Tonsilla Phase
Active ingredientSOLANUM DULCAMARA TOP, ECHINACEA ANGUSTIFOLIA, HORSE CHESTNUT, ANTIMONY POTASSIUM TARTRATE, ASCORBIC ACID, PROTORTONIA CACTI, GALIUM APARINE, GENTIANA LUTEA ROOT, GERANIUM ROBERTIANUM, ANEMONE PRATENSIS, LACTIC ACID, L-, ACETYLCHOLINE CHLORIDE, MANNOSE, D-, CONIUM MACULATUM FLOWERING TOP, SUS SCROFA LYMPH, SULFUR, TRIBASIC CALCIUM PHOSPHATE, FERROSOFERRIC PHOSPHATE, SUS SCROFA UMBILICAL CORD, PORK LIVER, SUS SCROFA HYPOTHALAMUS, SUS SCROFA BONE MARROW, SUS SCROFA SPLEEN, CORTISONE ACETATE, SUS SCROFA ADRENAL GLAND, MERCURIUS SOLUBILIS, SUS SCROFA THYROID, BARIUM CARBONATE, SUS SCROFA TONSIL
Label structure9 sections

Dosage and administration

1-10 drops under the tongue, 2 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Dulcamara 4X, Echinacea (Angustifolia) 4X, Aesculus Hippocastanum 6X, Antimonium Tartaricum 6X, Ascorbicum Acidum 6X, Coccus Cacti 6X, Galium Aparine 6X, Gentiana Lutea 6X, Geranium Robertianum 6X, Pulsatilla (Vulgaris) 6X, Sarcolacticum Acidum 6X, Acetylcholine Chloride 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Mannose 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Conium Maculatum 8X, Lymph Node (Suis) 8X, Sulphur 8X, Calcarea Phosphorica 10X, Ferrum Phosphoricum 10X, Funiculus Umbilicalis Suis 10X, Hepar Suis 10X, Hypothalamus Suis 10X, Medulla Ossis Suis 10X, Thyroidinum (Suis) 13X, Baryta Carbonica 28X, Tonsil Suis 28X.

HOMEOPATHIC INDICATIONS:

OTC - PURPOSE SECTION

For the temporary relief of symptoms such as sore throat, pain, swelling, and inflammation.**

**These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

WARNING: Severe or persistent sore throat or sore throat accompanied by high fever, headache, nausea, and vomiting may be serious. Consult a physician promptly. Do not use more than two days or administer to children under 3 years of age unless directed by a physician.

WARNINGS:

WARNINGS SECTION

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

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

Tamper seal: "Sealed for Your Protection."

Do not use if seal is broken or missing.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

1-10 drops under the tongue, 2 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.

HOMEOPATHIC INDICATIONS:

INDICATIONS & USAGE SECTION

For the temporary relief of symptoms such as sore throat, pain, swelling, and inflammation.**

**These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

WARNING: Severe or persistent sore throat or sore throat accompanied by high fever, headache, nausea, and vomiting may be serious. Consult a physician promptly. Do not use more than two days or administer to children under 3 years of age unless directed by a physician.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Demineralized Water, 25% Ethanol

QUESTIONS:

OTC - QUESTIONS SECTION

Dist. By: Deseret Biologicals, Inc.

469 W. Parkland Drive

Sandy, UT 84070 www.desbio.com

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DESBIO
NDC 43742-1491-1
HOMEOPATHIC
BIO TONSILLA

PHASE
1 FL OZ (30 ml)

Bio Tonsilla PhaseBio Tonsilla Phase

Products#

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

DailyMed product names page 1 of 1 · 38 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43742-149143742-1491-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 31 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
44762423-53f6-4888-9fb1-a47a6965953397e735b4-752f-4e2e-a814-d87f295594672021-09-21WarningsExact identifier
spl id: 44762423-53f6-4888-9fb1-a47a69659533
spl set id: 97e735b4-752f-4e2e-a814-d87f29559467

Reported adverse events (FAERS/openFDA)#

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