NDC 51346-443 Snail Solu Tion Essence

Dimethicone

NDC Product Code 51346-443

NDC Code: 51346-443

Proprietary Name: Snail Solu Tion Essence What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Dimethicone What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

  • 51346 - Nature Republic Co., Ltd.
    • 51346-443 - Snail Solu Tion Essence

NDC 51346-443-02

Package Description: 1 BOTTLE, PUMP in 1 CARTON > 40 mL in 1 BOTTLE, PUMP (51346-443-01)

NDC Product Information

Snail Solu Tion Essence with NDC 51346-443 is a a human over the counter drug product labeled by Nature Republic Co., Ltd.. The generic name of Snail Solu Tion Essence is dimethicone. The product's dosage form is cream and is administered via topical form.

Labeler Name: Nature Republic Co., Ltd.

Dosage Form: Cream - An emulsion, semisolid3 dosage form, usually containing > 20% water and volatiles5 and/or < 50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.

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.

Snail Solu Tion Essence 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.

  • DIMETHICONE 1.07 g/40mL

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.

  • GLYCERIN (UNII: PDC6A3C0OX)
  • GLYCERETH-26 (UNII: NNE56F2N14)

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.

Product Labeler Information

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

Labeler Name: Nature Republic Co., Ltd.
Labeler Code: 51346
Marketing Category: UNAPPROVED DRUG OTHER - 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: 12-20-2016 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: 12-31-2019 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.

Snail Solu Tion Essence Product Label Images

Snail Solu Tion Essence 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 Ingredient

Active ingredients: DIMETHICONE 2.675

Inactive Ingredient

Inactive ingredients: SNAIL SECRETION FILTRATE,GLYCERIN,GLYCERETH-26,DIPROPYLENE GLYCOL,NIACINAMIDE,WATER,NEOPENTYL GLYCOL DIHEPTANOATE,CAPRYLIC/CAPRIC TRIGLYCERIDE,PENTYLENE GLYCOL,POLYSORBATE 80,ALCOHOL DENAT.,CYCLOMETHICONE,CYCLOPENTASILOXANE,DIPENTAERYTHRITYL HEXA C5-9 ACID ESTERS,TREHALOSE,HYDROGENATED LECITHIN,POLYSILICONE-11,PHENOXYETHANOL,SODIUM POLYACRYLATE,DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER,POLYPERFLUOROMETHYLISOPROPYL ETHER,FRAGRANCE(PARFUM),XANTHAN GUM,ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER,TROMETHAMINE,BUTYLENE GLYCOL,ADENOSINE,CARAMEL,POLOXAMER 188,PROPYLENE GLYCOL,HYDROLYZED CORN STARCH,DISODIUM EDTA,GLYCERYL ACRYLATE/ACRYLIC ACID COPOLYMER,1,2-HEXANEDIOL,SUCROSE,POTASSIUM CETYL PHOSPHATE,POLYPERFLUOROETHOXYMETHOXY DIFLUOROETHYL PEG PHOSPHATE,MADECASSOSIDE,CERAMIDE 3,ALGAE EXTRACT,CASSIA ANGUSTIFOLIA SEED POLYSACCHARIDE,VANILLA PLANIFOLIA FRUIT EXTRACT,POTASSIUM SORBATE,CITRIC ACID,CAPRYLHYDROXAMIC ACID

Purpose

Purpose: [SKIN PROTECTANT]

Cautions

CAUTIONS: For external use only. Avoid contact with eyes and mouth. Discontinue use if signs of irritation or rashes appear. Keep out of reach of children. Replace the cap after use.

Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN

How To Use

HOW TO USE: Apply an appropriate amount to the entire face and gently pat for absorption.

HOW TO USE: Apply an appropriate amount to the entire face and gently pat for absorption.

* Please review the disclaimer below.

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