NDC 50390-239 Artistry Youth Xtend Lifting Smoothing Foundation Shade Chiffon L2c1

Octinoxate, Oxybenzone

NDC Product Code 50390-239

NDC CODE: 50390-239

Proprietary Name: Artistry Youth Xtend Lifting Smoothing Foundation Shade Chiffon L2c1 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.

Non-Proprietary Name: Octinoxate, Oxybenzone 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.

NDC Code Structure

  • 50390 - Amway Corp
    • 50390-239 - Artistry Youth Xtend Lifting Smoothing Foundation Shade Chiffon

NDC 50390-239-00

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

NDC Product Information

Artistry Youth Xtend Lifting Smoothing Foundation Shade Chiffon L2c1 with NDC 50390-239 is a 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.

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.

Artistry Youth Xtend Lifting Smoothing Foundation Shade Chiffon L2c1 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.


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.

  • CHLORELLA VULGARIS (UNII: RYQ4R60M02)
  • SOYBEAN OIL (UNII: 241ATL177A)
  • CERAMIDE NP (UNII: 4370DF050B)
  • MEADOWFOAM SEED OIL (UNII: 412ZHA4T4Y)
  • .BETA.-SITOSTEROL (UNII: S347WMO6M4)
  • PERILLA FRUTESCENS SEED OIL (UNII: 322MS57V7Z)
  • CHIA SEED OIL (UNII: MC2LH51BO7)
  • EVENING PRIMROSE OIL (UNII: 3Q9L08K71N)
  • TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
  • WATER (UNII: 059QF0KO0R)
  • CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
  • METHYL TRIMETHICONE (UNII: S73ZQI0GXM)
  • BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • LAURYL PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE (UNII: 25G622K2RA)
  • TALC (UNII: 7SEV7J4R1U)
  • DIMETHICONE (UNII: 92RU3N3Y1O)
  • TRIMETHYLOLPROPANE TRICAPRYLATE/TRICAPRATE (UNII: N1TRQ06KVJ)
  • POLYGLYCERYL-6 POLYRICINOLEATE (UNII: YPM0ZOC2HR)
  • HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)
  • DIMETHICONE/PEG-10/15 CROSSPOLYMER (UNII: 21AS8B1BSS)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • SODIUM CHLORIDE (UNII: 451W47IQ8X)
  • SODIUM CITRATE (UNII: 1Q73Q2JULR)
  • TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
  • ALUMINUM OXIDE (UNII: LMI26O6933)
  • SORBITAN MONOLAURATE (UNII: 6W9PS8B71J)
  • ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
  • STEARIC ACID (UNII: 4ELV7Z65AP)
  • METHYLPARABEN (UNII: A2I8C7HI9T)
  • HYALURONATE SODIUM (UNII: YSE9PPT4TH)
  • PROPYLPARABEN (UNII: Z8IX2SC1OH)
  • HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)
  • ACETYL TYROSYLARGININE CETYL ESTER (UNII: 3M7W78X5IR)
  • ETHYLPARABEN (UNII: 14255EXE39)
  • SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
  • IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)

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: Amway Corp
Labeler Code: 50390
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: 05-06-2013 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: 12-31-2022 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.

Artistry Youth Xtend Lifting Smoothing Foundation Shade Chiffon L2c1 Product Label Images

Artistry Youth Xtend Lifting Smoothing Foundation Shade Chiffon L2c1 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 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 useApply liberally 15 minutes before sun exposureUse a water resistant sunscreen if swimming or sweating or washingReapply at least every 2 hoursSun 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 sunglassesChildren 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

* Please review the disclaimer below.