NDC 73590-0060 Multi-function Smart Bb Spf30 Pa

Titanium Dioxide

NDC Product Code 73590-0060

NDC 73590-0060-1

Package Description: 30 mL in 1 TUBE

NDC Product Information

Multi-function Smart Bb Spf30 Pa with NDC 73590-0060 is a a human over the counter drug product labeled by Noksibcho Cosmetic Co., Ltd.. The generic name of Multi-function Smart Bb Spf30 Pa is titanium dioxide. The product's dosage form is cream and is administered via topical form.

Labeler Name: Noksibcho Cosmetic 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.

Multi-function Smart Bb Spf30 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 5.9 g/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.

  • HYALURONATE SODIUM (UNII: YSE9PPT4TH)
  • GLYCERIN (UNII: PDC6A3C0OX)

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: Noksibcho Cosmetic Co., Ltd.
Labeler Code: 73590
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: 09-07-2020 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.

Multi-function Smart Bb Spf30 Pa Product Label Images

Multi-function Smart Bb Spf30 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

Talc

Silica

Mineral Oil

Triethoxycaprylylsilane

Dimethiconol Stearate

Dimethicone

Cyclomethicone

Cetyl Ethylhexanoate

Ethylhexyl Methoxycinnamate

titanium dioxide

Aluminum hydroxide

Stearic acid

Cyclomethicone

PEG-10 Dimethicone

Isohexadecane

zinc oxide

Methicone

Cyclomethicone

PEG-10 Dimethicone

Glycerin

Dimethicone

Dimethicone/Vinyl Dimethicone Crosspolymer

Butylene Glycol Dicaprylate/Dicaprate

Dipropylene Glycol

Cetyl PEG/PPG-10/1 Dimethicone

4-Methylbenzylidene Camphor

PEG-10 Dimethicone

Squalane

Arbutin

Isoamyl p-Methoxycinnamate

Disteardimonium Hectorite

Magnesium Sulfate

Phenoxyethanol

Aloe Barbadensis Leaf Extract

Paeonia Lactiflora Extract

Lilium Tigrinum Extract

Solanum Lycopersicum (Tomato) Fruit Extract

Camellia Sinensis Leaf Extract

Adenosine

Sodium Hyaluronate

Methyl paraben

Leontopodium alpinum extract

Malva Sylvestris (Mallow) Flower Extract

CI 77492

CI 77491

CI 77499

Parfum

Otc - Purpose

Sun block

Otc - Keep Out Of Reach Of Children

Keep out of reach of the children

Indications & Usage

1. Use your regular skin care products to smooth the skin texture.

2. Apply a small amount of Multi Function Smart BB Cream to your face.

3. Spread it softly on your whole face.

4. Be confident with the brighter skin tone!

Warnings

For external use only

When using this product
■ if the following symptoms occurs after use, stop use and consult with a skin specialistred specks, swelling, itching■ don’t use on the part where there is injury, eczema, or dermatitisKeep out of reach of children■ if swallowed, get medical help or contact a person control center immediately

* Please review the disclaimer below.