NDC 10893-520 Naturasil Skin Tags

Thuja Occidentalis

NDC Product Code 10893-520

NDC 10893-520-15

Package Description: 1 LIQUID in 1 BOTTLE, GLASS

NDC 10893-520-30

Package Description: 1 LIQUID in 1 BOTTLE, GLASS

NDC 10893-520-50

Package Description: 1 LIQUID in 1 BOTTLE, GLASS

NDC Product Information

Naturasil Skin Tags with NDC 10893-520 is a a human over the counter drug product labeled by Nature's Innovation, Inc.. The generic name of Naturasil Skin Tags is thuja occidentalis. The product's dosage form is liquid and is administered via topical form.

Labeler Name: Nature's Innovation, Inc.

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Naturasil Skin Tags Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • THUJA OCCIDENTALIS LEAFY TWIG 6 [hp_X]/1
  • THUJA OCCIDENTALIS LEAFY TWIG 6 [hp_X]/1

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • CEDAR LEAF OIL (UNII: BJ169U4NLG)
  • TEA TREE OIL (UNII: VIF565UC2G)
  • CASTOR OIL (UNII: D5340Y2I9G)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Nature's Innovation, Inc.
Labeler Code: 10893
Marketing Category: UNAPPROVED HOMEOPATHIC - What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 10-01-2011 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2022 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: N - NO What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Naturasil Skin Tags Product Label Images

Naturasil Skin Tags Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Otc - Active Ingredient

Drug FactsActive Ingredients:Thuja Occidentalis 6X HPUS

Description

The letters HPUS indicate the component(s) in this product is (are) officially monographed in the Homeopathic Pharmacopeia of the United States.

Otc - Purpose

PurposePolypi, 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 866.371.2499 Mfd. by: Nature'sInnovation, Inc. 2723 Brickton North Dr., Buford, GA 30518 Not tested on animals.

* Please review the disclaimer below.