NDC 10893-610 Naturasil Molluscum Relief

Sulfur, Thuja Occindentalis

NDC Product Code 10893-610

NDC 10893-610-04

Package Description: 113.3 g in 1 CARTON

NDC Product Information

Naturasil Molluscum Relief with NDC 10893-610 is a a human over the counter drug product labeled by Natures Innovation, Inc.. The generic name of Naturasil Molluscum Relief is sulfur, thuja occindentalis. The product's dosage form is soap and is administered via topical form.

Labeler Name: Natures Innovation, Inc.

Dosage Form: Soap - Any compound of one or more fatty acids, or their equivalents, with an alkali; soap is detergent and is much employed in liniments, enemas, and in making pills. It is also a mild aperient, antacid and antiseptic.

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 Molluscum Relief 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.

  • SULFUR 1 [hp_X]/113.3g
  • THUJA OCCIDENTALIS LEAF 6 [hp_X]/113.3g

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.

  • WATER (UNII: 059QF0KO0R)
  • CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
  • COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
  • COCONUT OIL (UNII: Q9L0O73W7L)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • GLYCERYL LAURATE (UNII: Y98611C087)
  • LAVENDER OIL (UNII: ZBP1YXW0H8)
  • PENTASODIUM PENTETATE (UNII: 961TOZ5L7T)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • SODIUM CHLORIDE (UNII: 451W47IQ8X)
  • SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)
  • SODIUM LAURATE (UNII: K146MR5EXO)
  • SODIUM MYRISTATE (UNII: 06BLC4V0IV)
  • SODIUM OLEATE (UNII: 399SL044HN)
  • SODIUM STEARATE (UNII: QU7E2XA9TG)
  • SODIUM THIOSULFATE (UNII: HX1032V43M)
  • SORBITOL (UNII: 506T60A25R)
  • ETIDRONATE TETRASODIUM (UNII: CZZ9T1T1X4)
  • TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
  • TRISODIUM SULFOSUCCINATE (UNII: 085WB9L09N)

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: Natures 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: 10-22-2020 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: 12-31-2021 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 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Naturasil Molluscum Relief Product Label Images

Naturasil Molluscum Relief 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

Active Ingredients:

Sulfur 1X HPUS, Thuja Occindentalis 6X HPUS*.The letters HPUS indicate the component(s) in this product is (are) officially monographed in the Homeopathic Pharmacopeia of the United States.

Purpose:

Molluscum Contagiosum Symptom Relief.

Uses:

Symptomatic homeopathic topical treatment of common molluscum contagiosum.

Warnings:

For external use only. Ask a doctor before use if pregnant or nursing. Avoid using near eyes, mouth or mucous membranes. If contact with eyes or mucous membranes occurs, rinse thoroughly with water.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. In case of ingestion, call Poison Control Center hotline immediately at 1-800-222-1222

Directions:

Use soap at least 2 times per day, for 4-10 days. Drying of skin may occur. Some individuals may be sensitive to essential oils. Skin test for tolerability. If irritation or reaction occurs, discontinue use.

Inactive Ingredients:

Aqua, Citric Acid, Cocamidopropyl Betaine, Cocos Nucifera (coconut oil), Glycerin, Glyceryl Laurate, Lavender Oil, Pentasodium Pentetate, Propylene Glycol, Sodium Chloride, Sodium Citrate, Sodium Laurate, Sodium Myristate, Sodium Oleate, Sodium Stearate, Sodium Thiosulfate, Sorbitol, Tetrasodium Etidronate, Titanium Dioxide, Trisodium Sulfosuccinate.

* Please review the disclaimer below.