Warts - Moles - Skin Tags

Manufacturer
Newton Laboratories, Inc.
Effective date
2020-01-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:42:34

Label at a glance#

ProductWarts - Moles - Skin Tags
Active ingredientANTIMONY TRISULFIDE, BRYONIA ALBA ROOT, OYSTER SHELL CALCIUM CARBONATE, CRUDE, CAUSTICUM, SOLANUM DULCAMARA TOP, GRAPHITE, LYCOPODIUM CLAVATUM SPORE, MERCURIC SULFIDE, SODIUM CARBONATE, NITRIC ACID, STRYCHNOS NUX-VOMICA SEED, TOXICODENDRON PUBESCENS LEAF, JUNIPERUS SABINA LEAFY TWIG, SEPIA OFFICINALIS JUICE, SILICON DIOXIDE, DELPHINIUM STAPHISAGRIA SEED, SULFUR, THUJA OCCIDENTALIS LEAFY TWIG, TARAXACUM OFFICINALE
Label structure10 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Formulated for warts (including genital), moles, keloids, molluscum and skin tags.

DOSAGE & ADMINISTRATION SECTION

Directions: Ages 12 and up, take 6 pellets by mouth (ages 0 to 11, give 3 pellets) one to four times daily or as directed by a health professional. Under age 2, crush/dissolve pellets in purified water. Sensitive persons begins with 1 pellet and gradually increase to full dose.

OTC - ACTIVE INGREDIENT SECTION

Equal parts of Taraxacum 6x, Thuja occ. 6x, Antimon. crud. 15x, Bryonia 15x, Calc.carb. 15x, Causticum 15x, Dulcamara 15x, Graphites 15x, Lycopodium 15x, Merc. sulph. rub. 15x, Nat. carb. 15x, Nitricum ac.15x, Nux vom. 15x, Rhus toxicodendron 15x, Sabina 15x, Sepia 15x, Silicea 15x, Staphysag. 15x, Sulphur 15x, Thuja occ. 15x.

OTC - PURPOSE SECTION

Formulated for warts (including genital), moles, keloids, molluscum and skin tags.

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Gluten-free, non-GMO, beet-derived sucrose (lactose-free) pellets.

QUESTIONS SECTION

OTC - QUESTIONS SECTION

newtonlabs.net – Questions? 800.448.7256

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

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.

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

PACKAGE LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package labelpackage label

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55714-254355714-2543-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 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
0b50233d-0fce-efc0-e063-6294a90ac4429d4ac337-5f4b-ef47-e053-2a95a90a6dbf2023-11-29WarningsExact identifier
spl set id: 9d4ac337-5f4b-ef47-e053-2a95a90a6dbf

Reported adverse events (FAERS/openFDA)#

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