Candida - Yeast

Manufacturer
Newton Laboratories, Inc.
Effective date
2020-11-24
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 23:05:45

Label at a glance#

ProductCandida - Yeast
Active ingredientEPINEPHRINE, CANDIDA ALBICANS, THYROID, UNSPECIFIED, SACCHAROMYCES CEREVISIAE, ELYMUS REPENS ROOT, USTILAGO MAYDIS, ANTIMONY TRISULFIDE, ARSENIC TRIOXIDE, BAPTISIA TINCTORIA, MAHONIA AQUIFOLIUM ROOT BARK, BRYONIA ALBA ROOT, TRIBASIC CALCIUM PHOSPHATE, CINCHONA OFFICINALIS BARK, CHAMAELIRIUM LUTEUM ROOT, GOLDENSEAL, IODINE, IRIS VERSICOLOR ROOT, POTASSIUM CARBONATE, LACHESIS MUTA VENOM, LYCOPODIUM CLAVATUM SPORE, MERCURY, SODIUM CARBONATE, SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE, NITRIC ACID, SEPIA OFFICINALIS JUICE, PHOSPHORUS, PODOPHYLLUM, PULSATILLA VULGARIS, ECHINACEA, UNSPECIFIED, GINKGO, ENGLISH WALNUT, ARCTIUM LAPPA ROOT, THUJA OCCIDENTALIS LEAFY TWIG
Label structure10 sections

Label contents#

Full prescribing information#

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

INACTIVE INGREDIENT SECTION

USP Purified water; USP Gluten-free, non-GMO, organic cane alcohol 20%

OTC - PURPOSE SECTION

Formulated for associated symptoms such as gas, bloating, fatigue, mental fogginess, itching, discharge and other related symptoms.

WARNINGS SECTION

WARNINGS: Keep out of reach of children. Do not use if tamper-evident seal is broken or missing. If symptoms worsen or persist for more than a few days, consult a doctor. If pregnant or breast-feeding, ask a doctor before use.

QUESTIONS SECTION

OTC - QUESTIONS SECTION

newtonlabs.net - Questions? 800 448-7256

Newton Laboratories, Inc. FDA Est # 1051203 - Conyers, GA 30013

OTC - ACTIVE INGREDIENT SECTION

Equal parts of Echinacea 6x, Ginkgo 6x, Juglans reg. 6x, Lappa 6x, Thuja occ. 6x, Antimon. crud. 10x, Baptisia 10x, Berber. aqui. 10x, Bryonia 10x, Calc. phos. 10x, Cinchona 10x, Helonias 10x, Hydrastis 10x, Iodium 10x, Iris vers. 10x, Kali carb. 10x, Lachesis 10x, Lycopodium 10x, Merc. viv. 10x, Nat.carb. 10x, Nat. phos. 10x, Nitricum ac. 10x, Phos. 10x, Podoph. pelt. 10x, Pulsatilla 10x, Sepia 10x, Adrenalinum 15x, Arsenium alb. 15x, Candida alb. 15x, Thyroidinum 15x, Torula cerevisiae 15x, Triticum 15x, Ustilago maidis 15x.

DOSAGE & ADMINISTRATION SECTION

Ages 12 and up, take 6 drops by mouth (ages 0 to 11, give 3 drops) one to four times daily or as directed by a health professional.

Sensitive persons begin with 1 drop and gradually increase to full dose.

INDICATIONS & USAGE SECTION

Formulated for associated symptoms such as gas, bloating, fatigue, mental fogginess, itching, discharge and other related symptoms.

PACKAGE LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package labelpackage label

FDA-Initiated Inactive NDC Indexing#

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55714-240055714-2400-0, 55714-2400-1, 55714-2400-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 35 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
10a6f559-2c87-d494-e063-6294a90ace197a06a959-96ca-6b87-e053-2991aa0aabe12024-02-05WarningsExact identifier
spl set id: 7a06a959-96ca-6b87-e053-2991aa0aabe1

Reported adverse events (FAERS/openFDA)#

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