NDC 14783-039 Lbel Paris Regression Jour

NDC Product Code 14783-039

NDC 14783-039-51

Package Description: 1 JAR in 1 BOX > 5 g in 1 JAR (14783-039-52)

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

NDC Product Information

Lbel Paris Regression Jour with NDC 14783-039 is a product labeled by Ventura International Ltd. The generic name of Lbel Paris Regression Jour is . The product's dosage form is and is administered via form.

Labeler Name: Ventura International Ltd

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)
  • SOYBEAN (UNII: L7HT8F1ZOD)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
  • CETYL ALCOHOL (UNII: 936JST6JCN)
  • C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
  • SNOW PEA (UNII: 84SKC33B1I)
  • CYCLOMETHICONE 6 (UNII: XHK3U310BA)
  • TROLAMINE (UNII: 9O3K93S3TK)
  • GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
  • MANNITOL (UNII: 3OWL53L36A)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • STEARIC ACID (UNII: 4ELV7Z65AP)
  • METHYLPARABEN (UNII: A2I8C7HI9T)
  • C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
  • PROPYLPARABEN (UNII: Z8IX2SC1OH)
  • XANTHAN GUM (UNII: TTV12P4NEE)
  • CETETH-20 (UNII: I835H2IHHX)
  • STEARETH-20 (UNII: L0Q8IK9E08)
  • EDETATE DISODIUM (UNII: 7FLD91C86K)
  • LAURETH-7 (UNII: Z95S6G8201)
  • YEAST (UNII: 3NY3SM6B8U)
  • DIMETHICONE (UNII: 92RU3N3Y1O)
  • BUTYLPARABEN (UNII: 3QPI1U3FV8)
  • ETHYLPARABEN (UNII: 14255EXE39)
  • ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
  • LAURETH-23 (UNII: N72LMW566G)
  • LAURETH-4 (UNII: 6HQ855798J)
  • SODIUM SUCCINATE ANHYDROUS (UNII: V8ZGC8ISR3)
  • WATER (UNII: 059QF0KO0R)
  • SOYBEAN (UNII: L7HT8F1ZOD)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
  • CETYL ALCOHOL (UNII: 936JST6JCN)
  • C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
  • SNOW PEA (UNII: 84SKC33B1I)
  • CYCLOMETHICONE 6 (UNII: XHK3U310BA)
  • TROLAMINE (UNII: 9O3K93S3TK)
  • GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
  • MANNITOL (UNII: 3OWL53L36A)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • STEARIC ACID (UNII: 4ELV7Z65AP)
  • METHYLPARABEN (UNII: A2I8C7HI9T)
  • C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
  • PROPYLPARABEN (UNII: Z8IX2SC1OH)
  • XANTHAN GUM (UNII: TTV12P4NEE)
  • CETETH-20 (UNII: I835H2IHHX)
  • STEARETH-20 (UNII: L0Q8IK9E08)
  • EDETATE DISODIUM (UNII: 7FLD91C86K)
  • LAURETH-7 (UNII: Z95S6G8201)
  • YEAST (UNII: 3NY3SM6B8U)
  • DIMETHICONE (UNII: 92RU3N3Y1O)
  • BUTYLPARABEN (UNII: 3QPI1U3FV8)
  • ETHYLPARABEN (UNII: 14255EXE39)
  • ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
  • LAURETH-23 (UNII: N72LMW566G)
  • LAURETH-4 (UNII: 6HQ855798J)
  • SODIUM SUCCINATE ANHYDROUS (UNII: V8ZGC8ISR3)

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 Ltd
Labeler Code: 14783
Start Marketing Date: 08-15-2010 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 Paris Regression Jour 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

Avobenzone (2 %), Ensulizole (1 %), Octinoxate (7.5 %), Oxybenzone (2 %)

Purpose

Sunscreen

Uses

  • Helps prevent sunburnhigher SPF gives more sunburn protectionprovides moderate protection against sunburn

Warnings

  • For external use only.

Directions

  • Apply smoothly every morning before sun exposure and as needed.apply after cleansing and toning on face and neck.children under 6 months of age: ask a doctor.

Other Information

  • Moderate sun protection product.Sun alert: Limiting sun exposure, wearing protective clothing, and using sunscreens may reduce the risk of skin cancer, and other harmful effects of the sun.

Inactive Ingredients

Aqua (water), glycine soja (soybean) protein, propylene glycol, cyclopentasiloxane, cetyl alcohol, c12-15 alkyl benzoate, pisum sativum (pea) extract, cyclohexasiloxane, triethanolamine, glyceryl stearate, mannitol, corn starch modified, polyacrylamide, phenoxyethanol, stearic acid, hydrolyzed adansonia digitata extract, peg-75 stearate, methylparaben, c13- 14 isoparaffin, propylparaben, xanthan gum, parfum (fragance), ceteth-20, steareth-20, pentaerythrityl tetra-di-t-butyl hydroxyhydrocinnamate, acrylates/c10-30 alkyl acrylate crosspolymer, disodium edta, laureth-7, cyclodextrin, dimethicone crosspolymer, faex extract (yeast extract), dimethicone, hydrolyzed algin, butylparaben, ethylparaben, chlorella vulgaris extract, maris aqua (sea water), isobutylparaben, laureth-23, laureth-4, disodium succinate, ci42090 (blue 1).

* Please review the disclaimer below.