Naturasil Liquid
FDA Label NDC 10893-520
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Nature's Innovation, Inc. for the product Naturasil (NDC 10893-520). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding otc - active ingredient, description, otc - purpose, indications & usage, warnings, otc - ask doctor, other safety information, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Description
Otc - Purpose
Purpose
Polypi, Naevi, Skin Tubercles Symptom Relief
Indications & Usage
Uses: Symptomatic treatment of skin tags. May be used for anal skin tags.
Warnings
Warnings: For external use only.
Otc - Ask Doctor
Ask a doctor before use if pregnant or nursing.
Other Safety Information
Avoid using near eyes or mouth.
In case of ingestion call Poison Control Center hotline immediately at 1-800-222-1222.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
Otc - Do Not Use
Do not use if tamper evident seal is broken.
Dosage & Administration
Directions: Apply 3 times daily to affected area. Skin tag will dry and flake away over a 3-6 week period. Some individuals may be sensitive to essential oils. Skin test for tolerability. If irritation or reaction occurs, discontinue use.
Inactive Ingredient
Inactive Ingredients: Cedar Leaf Oil, Melaleuca Alternifolia Leaf Oil, Ricinus Communis Seed Oil.
Otc - Questions
Questions? Comments?
www.naturasil.com 1-866-371-2499
Mfd. by: Nature's Innovation, Inc.,
2723 Brickton north Dr., Buford, GA 30518
Not tested on animals.
Package Label.Principal Display Panel
NDC# 10893-520-
100%
Natural Plant
Extracts
Naturasil10ml (.34 fl. oz.)
Topical Liquid
Homeopathic Medicine
Skin Tags
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