NDC 50390-239 Artistry Youth Xtend Lifting Smoothing Foundation Shade Chiffon L2c1
Octinoxate, Oxybenzone Cream Topical

Product Information

Artistry Youth Xtend Lifting Smoothing Foundation Shade Chiffon L2c1 is a human over the counter drug product labeled by Amway Corp. The generic name of Artistry Youth Xtend Lifting Smoothing Foundation Shade Chiffon L2c1 is octinoxate, oxybenzone. The product's dosage form is cream and is administered via topical form.

Product Code50390-239
Proprietary Name 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.
Artistry Youth Xtend Lifting Smoothing Foundation Shade Chiffon L2c1
Non-Proprietary Name 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.
Octinoxate, Oxybenzone
Product Type 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.
Human Otc Drug
Dosage FormCream - 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.
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.
Amway Corp
Labeler Code50390
FDA Application Number 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.
part352
Marketing Category 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.
OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
Start Marketing Date What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
05-06-2013
Listing Expiration Date 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.
12-31-2023
Exclude Flag 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".
N
NDC Code Structure

What are the uses for Artistry Youth Xtend Lifting Smoothing Foundation Shade Chiffon L2c1?


Product Packages

NDC 50390-239-00

Package Description: 1 BOTTLE, PLASTIC in 1 CARTON > 30 mL in 1 BOTTLE, PLASTIC

Product Details

What are Artistry Youth Xtend Lifting Smoothing Foundation Shade Chiffon L2c1 Active Ingredients?

An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

Artistry Youth Xtend Lifting Smoothing Foundation Shade Chiffon L2c1 Active Ingredients UNII Codes

Artistry Youth Xtend Lifting Smoothing Foundation Shade Chiffon L2c1 Inactive Ingredients UNII Codes

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.

* Please review the disclaimer below.

Artistry Youth Xtend Lifting Smoothing Foundation Shade Chiffon L2c1 Labeling and Warnings

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Table of Contents



Active Ingredients



Octinoxate 7.5% (W/W / P/P)

Oxybenzone 0.5% (W/W P/P)


Purpose



Sunscreen


Uses



  • Helps prevent sunburn

Warnings



For external use only


Do Not Use



on broken or damaged skin


When Using This Product



keep out of eyes. Rinse with water to remove.


Stop Use And Ask A Doctor



if rash occurs


Keep Out Of Reach Of Children.



If product is swallowed, get medical help or contact a Poison Control Center right away.


Directions



For suncreen use

  • Apply liberally 15 minutes before sun exposure
  • Use a water resistant sunscreen if swimming or sweating or washing
  • Reapply at least every 2 hours
  • Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging.
  • To decrease this risk, regularly use a sunscreen with a broad spectrum SPF of 15 or higher and other sun protection measures including:
  • limit time in the sun, especially from 10 a.m. – 2 p.m.
  • wear long-sleeve shirts, pants, hats, and sunglasses
  • Children under 6 months: ask a doctor

Other Information



  • Protect this product from excessive heat and direct sun

Inactive Ingredients



WATER/AQUA/EAU, CYCLOPENTASILOXANE, METHYL TRIMETHICONE, BUTYLENE GLYCOL, GLYCERIN, LAURYL PEG-9 POLYDIMETHYLSILOXYETHYL
DIMETHICONE, TALC, DIMETHICONE, TRIMETHYLOLPROPANE TRICAPRYLATE/TRICAPRATE, POLYGLYCERYL-6 POLYRICINOLEATE, HDI/
TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER, DIMETHICONE/PEG-10/15 CROSSPOLYMER, DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER, PHENOXYETHANOL, SODIUM CHLORIDE, SODIUM CITRATE, POLYGLYCERYL- 3 POLYDIMETHYLSILOXYETHYL DIMETHICONE, TRIETHOXYCAPRYLYLSILANE, ALUMINA, SORBITAN LAURATE, ALUMINUM HYDROXIDE, STEARIC ACID, METHYLPARABEN, SODIUM HYALURONATE, PROPYLPARABEN, FRAGRANCE/ PARFUM, HYDROXYETHYLCELLULOSE, ACETYL DIPEPTIDE-1 CETYL ESTER, ETHYLPARABEN, SILICA, IODOPROPYNYL BUTYLCARBAMATE, LECITHIN, CHLORELLA VULGARIS EXTRACT, GLYCINE SOJA (SOYBEAN) OIL, CERAMIDE-3, LIMNANTHES ALBA (MEADOWFOAM) SEED OIL, BETA-SITOSTEROL, PERILLA OCYMOIDES SEED OIL, SALVIA HISPANICA SEED OIL,
OENOTHERA BIENNIS (EVENING PRIMROSE) OIL, TETRAHEXYLDECYL ASCORBATE. MAY CONTAIN/PEUT CONTEINIR: TITANIUM DIOXIDE, IRON OXIDES, BISMUTH OXYCHLORIDE


Package Labeling:




* Please review the disclaimer below.