NDC 73329-0001 All About Soo Sun Stage Coolstick Spf50 Pa

Titanium Dioxide

NDC Product Code 73329-0001

NDC 73329-0001-1

Package Description: 20 g in 1 PACKAGE

NDC Product Information

All About Soo Sun Stage Coolstick Spf50 Pa with NDC 73329-0001 is a a human over the counter drug product labeled by All About Soo. The generic name of All About Soo Sun Stage Coolstick Spf50 Pa is titanium dioxide. The product's dosage form is stick and is administered via topical form.

Labeler Name: All About Soo

Dosage Form: Stick - A dosage form prepared in a relatively long and slender often cylindrical form.

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.

All About Soo Sun Stage Coolstick Spf50 Pa 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.

  • TITANIUM DIOXIDE .234 g/100g

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)
  • BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
  • DIMETHICONE (UNII: 92RU3N3Y1O)

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: All About Soo
Labeler Code: 73329
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 FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph. 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: 08-31-2019 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: 12-31-2020 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.

All About Soo Sun Stage Coolstick Spf50 Pa Product Label Images

All About Soo Sun Stage Coolstick Spf50 Pa 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

Titanium Dioxide

Inactive Ingredient

WATER

POLYETHYLENE

TRIHEPTANOIN

HOMOSALATE

ETHYLHEXYL METHOXYCINNAMATE

BHT

DIMETHICONE

ETHYLHEXYL SALICYLATE

POLYMETHYLSILSESQUIOXANE

METHYL METHACRYLATE CROSSPOLYMER

BUTYLENE GLYCOL

CETYL ETHYLHEXANOATE

SILICA DIMETHYL SILYLATE

POLYMETHYLSILSESQUIOXANE

SILICA

POLYHYDROXYSTEARIC ACID

TOCOPHERYL ACETATE

BIS-ETHYLHEXYLOXYPHENOL METHOXYPHENYL TRIAZINE

DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE

POLYGLYCERYL-4 DIISOSTEARATE/POLYHYDROXYSTEARATE/SEBACATE

OZOKERITE

DIMETHICONE

BISABOLOL

LAURYL POLYGLYCERYL-3 POLYDIMETHYLSILOXYETHYL DIMETHICONE

TOCOPHEROL

FRAGRANCE

CAPRYLYL GLYCOL

STEARIC ACID

ALUMINUM HYDROXIDE

GLYCERYL CAPRYLATE

MELIA AZADIRACHTA LEAF EXTRACT

MELIA AZADIRACHTA FLOWER EXTRACT

COCCINIA INDICA FRUIT EXTRACT

SOLANUM MELONGENA (EGGPLANT) FRUIT EXTRACT

ALOE BARBADENSIS FLOWER EXTRACT

SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL

OCIMUM SANCTUM LEAF EXTRACT

CORALLINA OFFICINALIS EXTRACT

CURCUMA LONGA (TURMERIC) ROOT EXTRACT

ETHYLHEXYLGLYCERIN

TOCOPHEROL

ALLANTOIN

WATER

BUTYLENE GLYCOL

ALOE BARBADENSIS LEAF EXTRACT

PENTYLENE GLYCOL

1,2-HEXANEDIOL

CAPRYLYL GLYCOL

WATER

PENTYLENE GLYCOL

CENTELLA ASIATICA EXTRACT

ETHYLHEXYLGLYCERIN

WATER

1,2-HEXANEDIOL

WATER

DIPROPYLENE GLYCOL

1,2-HEXANEDIOL

MENTHA AQUATICA EXTRACT

Otc - Purpose

Brightens your skin. Enhances wrinkles Protects the skin against UV rays. (SPF50+,PA++++)

Otc - Keep Out Of Reach Of Children

Keep out of reach of the children

Indications & Usage

As the last step of skin care, turn the dial on

the bottom of container to raise content about 5 millimeters

and apply on areas that need UV protection (face, body).

Usage/Volume Take an appropriate amount of this pro

-duct and apply it evenly on the skin.

Warnings

1. While using this product , if there

is any abnormal symptoms or side effect such as red spot,

swelling or itching, please consult with dermatologist.

2. Do not use in areas with wounds 3. Instructions for sto

-rage and usage. (i) Keep out of reach of infants and chil

-dren (ii) Store it in a place away from direct sunlight

Dosage & Administration

For external use only

* Please review the disclaimer below.