NDC 77049-0006 Skin Delight Hand Washgel


NDC Product Code 77049-0006

NDC 77049-0006-1

Package Description: 500 mL in 1 BOTTLE

NDC Product Information

Skin Delight Hand Washgel with NDC 77049-0006 is a a human over the counter drug product labeled by Interkos Co., Ltd.. The generic name of Skin Delight Hand Washgel is alcohol. The product's dosage form is gel and is administered via topical form.

Labeler Name: Interkos Co., Ltd.

Dosage Form: Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.

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.

Skin Delight Hand Washgel 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.

  • ALCOHOL 61.75 mL/100mL

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.

  • CARBOMER 940 (UNII: 4Q93RCW27E)
  • WATER (UNII: 059QF0KO0R)

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: Interkos Co., Ltd.
Labeler Code: 77049
FDA Application Number: part333A What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

Marketing Category: OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final. 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: 10-23-2020 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 - 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.

Skin Delight Hand Washgel Product Label Images

Skin Delight Hand Washgel 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


Inactive Ingredient




PEG-60 Hydrogenated Castor Oil




Butylene Glycol

Salix Alba (Willow) Bark Extract

Origanum Vulgare Leaf Extract

Chamaecyparis Obtusa Leaf Extract

Portulaca Oleracea Extract

Lactobacillus/Soybean Ferment Extract

Cinnamomum Cassia Bark Extract

Scutellaria Baicalensis Root Extract

Vincetoxicum Atratum Extract


Caprylyl Glycol

Aloe Barbadensis Leaf Extract

Illicium Verum (Anise) Fruit Extract

Otc - Purpose

Protecting hands from the harmful environment and keeping hands healthy and clean with feeling sense the freshness without stinckness.

Otc - Keep Out Of Reach Of Children


Indications & Usage

Share some portion onto the palm and evenly spread it.


1. If any one of following symptoms occurs when using cosmetics, stop using it and consult a dermatologist.

A.red spot. swelling, itching, stimulus.

B.symptoms mentioned above are caused by sunlight.

2. Do not apply on skin where there is wound, eczema, or irritation.

3. Do not use for the purpose other than indicated.

4. Storage and cautions for handling.

A. keep out of reach of children.

B.keep away from direct sunlight.

Dosage & Administration

For external use only

* Please review the disclaimer below.