NDC 58411-205 Cle De Peau Beaute Correcting Veil

NDC Product Code 58411-205

NDC CODE: 58411-205

Proprietary Name: Cle De Peau Beaute Correcting Veil 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.

NDC Code Structure

  • 58411 - Shiseido Americas Corporation
    • 58411-205 - Cle De Peau Beaute Correcting Veil

NDC 58411-205-60

Package Description: 1 TUBE in 1 CARTON > 36 mL in 1 TUBE

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Cle De Peau Beaute Correcting Veil with NDC 58411-205 is a product labeled by Shiseido Americas Corporation. The product's dosage form is and is administered via form.

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)
  • DIMETHICONE (UNII: 92RU3N3Y1O)
  • BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • ISOHEXADECANE (UNII: 918X1OUF1E)
  • POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69)
  • PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE (UNII: TYP81E471F)
  • NYLON-12 (UNII: 446U8J075B)
  • TRIISOSTEARIN (UNII: 71503RH8KG)
  • DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
  • ERYTHRITOL (UNII: RA96B954X6)
  • CETYL ETHYLHEXANOATE (UNII: 134647WMX4)
  • XYLITOL (UNII: VCQ006KQ1E)
  • SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
  • ISODECYL NEOPENTANOATE (UNII: W60VYE24XC)
  • TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN)
  • SODIUM ACETYLATED HYALURONATE (UNII: WN66R7GL93)
  • ROSA ROXBURGHII FRUIT (UNII: CVT1AA87FF)
  • TROLAMINE (UNII: 9O3K93S3TK)
  • ISOSTEARIC ACID (UNII: X33R8U0062)
  • ALUMINUM DISTEARATE (UNII: 7P1HP1B9UI)
  • ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
  • EDETATE DISODIUM (UNII: 7FLD91C86K)
  • ALUMINUM OXIDE (UNII: LMI26O6933)
  • BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
  • TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
  • .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
  • ALCOHOL (UNII: 3K9958V90M)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • FERRIC OXIDE RED (UNII: 1K09F3G675)
  • FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
  • MICA (UNII: V8A1AW0880)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Shiseido Americas Corporation
Labeler Code: 58411
Start Marketing Date: 09-01-2014 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: I - INACTIVATED, the listing data was inactivated by the FDA. 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.

Cle De Peau Beaute Correcting Veil Product Label Images

Cle De Peau Beaute Correcting Veil 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 - Purpose

Active ingredientsPurposeENSULIZOLE 1.0%SunscreenOCTINOXATE 2.9%SunscreenTITANIUM DIOXIDE 2.4%Sunscreen

Uses

  • Helps prevent sunburnif used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun

Warnings

For external use only

Otc - Do Not Use

Do not use on damaged or broken skin

Otc - When Using

When using this product keep out of eyes. Rinse with water to remove.

Otc - Stop Use

Stop use and ask a doctor if rash occurs

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • For sunscreen use:apply liberally 15 minutes before sun exposureuse a water resistant sunscreen if swimming or sweatingreapply 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 sunglasseschildren under 6 months: Ask a doctor

Inactive Ingredients

WATER∙DIMETHICONE∙BUTYLENE GLYCOL∙GLYCERIN∙ISOHEXADECANE∙SD ALCOHOL 40-B∙POLYMETHYLSILSESQUIOXANE∙PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE∙NYLON-12∙TRIISOSTEARIN∙DISTEARDIMONIUM HECTORITE∙ERYTHRITOL∙CETYL ETHYLHEXANOATE∙XYLITOL∙SILICA∙ISODECYL NEOPENTANOATE∙TRIMETHYLSILOXYSILICATE∙SODIUM ACETYLATED HYALURONATE∙ROSA ROXBURGHII FRUIT EXTRACT∙DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER∙HYDROLYZED CONCHIOLIN PROTEIN∙HYDROLYZED SILK∙TRIETHANOLAMINE∙ISOSTEARIC ACID∙ALUMINUM DISTEARATE∙ALUMINUM HYDROXIDE∙DISODIUM EDTA∙ALUMINA∙BHT∙TRIETHOXYCAPRYLYLSILANE∙TOCOPHEROL∙POLYSILICONE-2∙ALCOHOL∙PHENOXYETHANOL∙FRAGRANCE∙TITANIUM DIOXIDE∙IRON OXIDES∙MICA∙

Other Information

  • Protect this product in this container from excessive heat and direct sun.

* Please review the disclaimer below.