NDC 14783-990 Lbel Couleur Luxe Rouge Irresistible

NDC Product Code 14783-990

NDC CODE: 14783-990

Proprietary Name: Lbel Couleur Luxe Rouge Irresistible 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

NDC 14783-990-05

Package Description: 12 TUBE in 1 CARTON > 4 g in 1 TUBE (14783-990-04)

NDC 14783-990-12

Package Description: 12 TRAY in 1 CARTON > 11.4 g in 1 TRAY (14783-990-11)

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

NDC Product Information

Lbel Couleur Luxe Rouge Irresistible with NDC 14783-990 is a product labeled by Ventura International, Limited. 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.

  • ETHYLHEXYL PALMITATE (UNII: 2865993309)
  • SHEA BUTTER (UNII: K49155WL9Y)
  • CERESIN (UNII: Q1LS2UJO3A)
  • CARNAUBA WAX (UNII: R12CBM0EIZ)
  • TRIDECYL STEARATE (UNII: A8OE252M6L)
  • OCTYLDODECANOL (UNII: 461N1O614Y)
  • MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
  • PROPYLENE CARBONATE (UNII: 8D08K3S51E)
  • SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
  • METHYLPARABEN (UNII: A2I8C7HI9T)
  • PETROLATUM (UNII: 4T6H12BN9U)
  • BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
  • CHOLESTEROL (UNII: 97C5T2UQ7J)
  • BUTYLPARABEN (UNII: 3QPI1U3FV8)
  • ETHYLPARABEN (UNII: 14255EXE39)
  • BUTYLATED HYDROXYANISOLE (UNII: REK4960K2U)
  • CANDELILLA WAX (UNII: WL0328HX19)
  • YELLOW WAX (UNII: 2ZA36H0S2V)
  • CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
  • CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
  • PROPYLPARABEN (UNII: Z8IX2SC1OH)
  • ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
  • MICA (UNII: V8A1AW0880)
  • TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
  • ALUMINUM OXIDE (UNII: LMI26O6933)
  • D&C RED NO. 7 (UNII: ECW0LZ41X8)
  • FERRIC OXIDE RED (UNII: 1K09F3G675)
  • FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
  • FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
  • D&C RED NO. 30 (UNII: 2S42T2808B)
  • D&C RED NO. 21 (UNII: 08744Z6JNY)
  • BISMUTH OXYCHLORIDE (UNII: 4ZR792I587)
  • TALC (UNII: 7SEV7J4R1U)
  • FD&C RED NO. 40 (UNII: WZB9127XOA)
  • D&C BLUE NO. 4 (UNII: 0KSY80VYS3)
  • FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
  • PALMITIC ACID (UNII: 2V16EO95H1)

Product Labeler Information

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

Labeler Name: Ventura International, Limited
Labeler Code: 14783
Start Marketing Date: 11-26-2010 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 Couleur Luxe Rouge Irresistible Product Label Images

Lbel Couleur Luxe Rouge Irresistible 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 7.1 % , Oxybenzone 1.6%

Purpose

Sunscreen

Uses

Helps prevent sunburn

Otc - Stop Use

Stop use if skin rash occurs

Inactive Ingredients

Ethylhexyl palmitate, dipentaerythrityl hexacaprylate/hexacaprate, tridecyl trimellitate, polyethylene, polymethyl methacrylate, (butyrospermum parkii (shea butter), ozokerite, copernicia cerifera (carnauba) wax, tridecyl stearate, neopentyl glycol dicaprylate/dicaprate, octyldodecanol, disteardimonium hectorite, caprylic/capric triglyceride, phenoxyethanol, tocopheryl acetate, aloe barbadensis leaf extract, fragrance, microcrystalline wax, propylene carbonate, silica, methylparaben, petrolatum, phospholipids, bht, cholesterol, butylparaben, ethylparaben, crambe maritima extract, bha, euphorbia cerifera (candelilla) wax, beeswax, polyglyceryl-2 dipolyhydroxystearate, cetearyl glucoside, cetearyl alcohol, propylparaben, isobutylparaben, glycosphingolipids. May contain: mica, titanium dioxide, red 7 lake, iron oxides, yellow 5 lake, red 30 lake, red 21 lake, bismuth oxychloride, talc, red 40 lake, blue 1 lake, carmine, hydrogenated polyisobutene, palmitic acid.

Other

USA: Dist. by Ventura International Ltd. San Francisco, CA 94111. Made in Colombia. PUERTO RICO: Dist. by Ventura Corporation, Ltd., San Juan, Puerto Rico 00926. Made in Colombia.

* Please review the disclaimer below.