NDC 70930-105 Kocostar Sun Block Capsule Mask

Octinoxate, Octisalate, Titanium Dioxide

NDC Product Code 70930-105

NDC 70930-105-02

Package Description: 7 CONTAINER in 1 PACKAGE > 1.75 g in 1 CONTAINER (70930-105-01)

NDC Product Information

Kocostar Sun Block Capsule Mask with NDC 70930-105 is a a human over the counter drug product labeled by Natuzen Co.,ltd.. The generic name of Kocostar Sun Block Capsule Mask is octinoxate, octisalate, titanium dioxide. The product's dosage form is liquid and is administered via topical form.

Labeler Name: Natuzen Co.,ltd.

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.

Kocostar Sun Block Capsule Mask 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.

  • OCTINOXATE .13 g/1.75g
  • OCTISALATE .08 g/1.75g
  • TITANIUM DIOXIDE .06 g/1.75g

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.


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: Natuzen Co.,ltd.
Labeler Code: 70930
FDA Application Number: part352 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: 02-01-2020 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.

Kocostar Sun Block Capsule Mask Product Label Images

Kocostar Sun Block Capsule Mask 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


Inactive Ingredient

Inactive ingredients:Dimethicone, Cyclopentasiloxane, C12-15 Alkyl Benzoate, Polymethylsilsesquioxane, Dimethicone/Vinyl Dimethicone Crosspolymer, Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine, Isoamyl p-Methoxycinnamate, Dimethicone/PEG-10/15 Crosspolymer, Dimethicone Crosspolymer, Aluminum Stearate, Alumina, Polyhydroxystearic Acid, Phenoxyethanol, Fragrance, Tocopheryl Acetate, Limonene, Linalool, Hexyl Cinnamal, Salicornia Herbacea Extract, Phragmites Communis Extract, Benzyl Benzoate, Butylphenyl Methylpropional, Citronellol, Butylene Glycol, Glycerin, Benzyl Alcohol, Citral, Benzyl Salicylate, 1,2-Hexanediol


Purpose: Sunscreen


Warnings:● For external use only.● Use as directed.● Stop using the product and consult a dermatologist or physician if the following occurs: -swelling, red (strawberry) marks, or other abnormalities -itchiness due to indirect or direct exposure to light● Do not apply to open wounds, eczema, or dermatitis.● Avoid contact with eyes. if contact occurs, flush eyes thoroughly with clean and warm water.


Uses:Protect your skin from the SunDirections:1. Twist off the tip of a heart-shaped sunscreen capsule.2. Squeeze some amount of serum onto a fingertip.3. Apply the serum to the skin.

* Please review the disclaimer below.