NDC 13537-434 Lbel Effet Parfait Signs Of Age Appearance Minimizer Foundation Spf 20

  1. Labeler Index
  2. Ventura Corporation Ltd.
  3. NDC: 13537-434 Lbel Effet Parfait Signs Of Age Appearance Minimizer Foundation Spf 20

NDC Product Code 13537-434

NDC CODE: 13537-434

Proprietary Name: Lbel Effet Parfait Signs Of Age Appearance Minimizer Foundation Spf 20 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.

Drug Use Information

Drug Use Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.
  • This product is used as active ingredientspurposeoctinoxate 7.0 %sunscreentitanium dioxide 2.4 %sunscreen

NDC Code Structure

NDC 13537-434-02

Package Description: 1 BOTTLE in 1 BOX > 1 mL in 1 BOTTLE (13537-434-01)

NDC 13537-434-04

Package Description: 1 BOTTLE in 1 BOX > 3 mL in 1 BOTTLE (13537-434-03)

NDC 13537-434-06

Package Description: 1 BOTTLE in 1 BOX > 30 mL in 1 BOTTLE (13537-434-05)

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

NDC Product Information

Lbel Effet Parfait Signs Of Age Appearance Minimizer Foundation Spf 20 with NDC 13537-434 is product labeled by Ventura Corporation Ltd.. 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)
  • CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
  • DIMETHICONE (UNII: 92RU3N3Y1O)
  • CYCLOMETHICONE 6 (UNII: XHK3U310BA)
  • POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
  • HEXYL LAURATE (UNII: 4CG9F9W01Q)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • SODIUM CHLORIDE (UNII: 451W47IQ8X)
  • PEG/PPG-19/19 DIMETHICONE (UNII: EHH90CO7TL)
  • ARABICA COFFEE BEAN (UNII: 3SW678MX72)
  • PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • ALUMINUM OXIDE (UNII: LMI26O6933)
  • BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
  • DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
  • OCTYLDODECANOL (UNII: 461N1O614Y)
  • METHYLPARABEN (UNII: A2I8C7HI9T)
  • .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
  • PROPYLPARABEN (UNII: Z8IX2SC1OH)
  • BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
  • MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
  • BENZYL ALCOHOL (UNII: LKG8494WBH)
  • PETROLATUM (UNII: 4T6H12BN9U)
  • BUTYLPARABEN (UNII: 3QPI1U3FV8)
  • ETHYLPARABEN (UNII: 14255EXE39)
  • POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
  • ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
  • CHOLESTEROL (UNII: 97C5T2UQ7J)
  • POLYSORBATE 20 (UNII: 7T1F30V5YH)
  • CANDELILLA WAX (UNII: WL0328HX19)
  • YELLOW WAX (UNII: 2ZA36H0S2V)
  • CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
  • CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
  • CARNAUBA WAX (UNII: R12CBM0EIZ)
  • POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE (UNII: 9229XJ4V12)
  • PALMITOYL OLIGOPEPTIDE (UNII: HO4ZT5S86C)
  • PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R)
  • FERRIC OXIDE RED (UNII: 1K09F3G675)
  • FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
  • FERROSOFERRIC OXIDE (UNII: XM0M87F357)
  • TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)

Product Labeler Information

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

Labeler Name: Ventura Corporation Ltd.
Labeler Code: 13537
Start Marketing Date: 09-14-2012 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: 12-31-2017 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.

Lbel Effet Parfait Signs Of Age Appearance Minimizer Foundation Spf 20 Product Label Images

Lbel Effet Parfait Signs Of Age Appearance Minimizer Foundation Spf 20 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

Other

Drug Facts

  • Skin Cancer / Skin Aging Alert; Spending time in the sun increases your risk of skin cancer and early skin aging. This product has been shown only to help prevent sunburn, not skin cancer or early skin aging.

US: Dist. by Ventura International Ltd. DBA Belcorp USA, San Francisco, CA 94111

Otc - Purpose

Active IngredientsPurposeOctinoxate 7.0 %SunscreenTitanium Dioxide 2.4 %Sunscreen

Uses

  • Helps prevent sunburn

Otc - When Using

  • For external use only.

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

Otc - Do Not Use

  • Do not use on damage or broken skin.

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

Directions

  • Apply liberally and evenly 15 minutes before sun exposure.Children under 6 months of age: Ask a doctorReapply at least every 2 hoursUse a water resistant sunscreen if swimming or sweating.

Other Information

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

Inactive Ingredients

AQUA (WATER), CYCLOPENTASILOXANE, POLYMETHYL METHACRYLATE, DIMETHICONE, CYCLOHEXASILOXANE, CETYL PEG/PPG-10/1 DIMETHICONE, POLYGLYCERYL-4 ISOSTEARATE, HEXYL LAURATE, TRIMETHYLSILOXYSILICATE, GLYCERIN, SODIUM CHLORIDE, PEG/PPG-19/19 DIMETHICONE, Coffea Arabica (Coffee) Seedcake Extract, PEG/PPG-18/18 DIMETHICONE, PHENOXYETHANOL, ALUMINA, BUTYLENE GLYCOL, DIAZOLIDINYL UREA, OCTYLDODECANOL, METHYLPARABEN, TOCOPHERYL ACETATE, PROPYLPARABEN, METHICONE, BHT, MICROCRISTALLINA CERA (MICROCRYSTALLINE WAX), BENZYL ALCOHOL, PETROLATUM, BUTYLPARABEN, ETHYLPARABEN, PHOSPHOLIPIDS, POTASSIUM SORBATE, CARBOMER, ISOBUTYLPARABEN, CHOLESTEROL, POLYSORBATE 20, CANDELILLA CERA (EUPHORBIA CERIFERA (CANDELILLA) WAX), CERA ALBA (BEESWAX), CETEARYL ALCOHOL, CETEARYL GLUCOSIDE, COPERNICIA CERIFERA CERA (COPERNICIA CERIFERA (CARNAUBA ) WAX), POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE, GLYCOSPHINGOLIPIDS, PALMITOYL OLIGOPEPTIDE, PALMITOYL TETRAPEPTIDE-7, MAY CONTAIN: CI 77491 (IRON OXIDES), CI 77492 (IRON OXIDES), CI 77499 (IRON OXIDES), CI 77891 (TITANIUM DIOXIDE ), TRIETHOXYCAPRYLYLSILANE

* Please review the disclaimer below.