NDC 14783-304 Lbel Protege Expert

  1. Labeler Index
  2. Ventura International Ltd.
  3. NDC: 14783-304 Lbel Protege Expert

NDC Product Code 14783-304

NDC CODE: 14783-304

Proprietary Name: Lbel Protege Expert 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 sunscreen

NDC Code Structure

NDC 14783-304-02

Package Description: 1 BOTTLE in 1 BOX > 50 mL in 1 BOTTLE (14783-304-01)

NDC 14783-304-04

Package Description: 1 BOTTLE in 1 BOX > 5 mL in 1 BOTTLE (14783-304-03)

NDC 14783-304-05

Package Description: 1 mL in 1 PACKET

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

NDC Product Information

Lbel Protege Expert with NDC 14783-304 is product labeled by Ventura International 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)
  • DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
  • ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
  • DIMETHICONE (UNII: 92RU3N3Y1O)
  • CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
  • CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
  • SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
  • GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
  • POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
  • CYCLOMETHICONE 6 (UNII: XHK3U310BA)
  • SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
  • METHYLPARABEN (UNII: A2I8C7HI9T)
  • XANTHAN GUM (UNII: TTV12P4NEE)
  • MANNITOL (UNII: 3OWL53L36A)
  • PROPYLPARABEN (UNII: Z8IX2SC1OH)
  • BUTYLPARABEN (UNII: 3QPI1U3FV8)
  • ETHYLPARABEN (UNII: 14255EXE39)
  • ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
  • ARGININE (UNII: 94ZLA3W45F)
  • YEAST (UNII: 3NY3SM6B8U)
  • HISTIDINE MONOHYDROCHLORIDE (UNII: 1D5Q932XM6)
  • PEA (UNII: W4X7H8GYFM)
  • SODIUM SUCCINATE ANHYDROUS (UNII: V8ZGC8ISR3)
  • KHAYA SENEGALENSIS BARK (UNII: 1S7EDA839L)
  • NADIDE (UNII: 0U46U6E8UK)
  • PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)
  • ASPARTIC ACID (UNII: 30KYC7MIAI)

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: 04-19-2011 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 Protege Expert Product Label Images

Lbel Protege Expert 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

Ensulizole 3%, Octinoxate 7.5%, Octisalate 5%, Oxybenzone 6%, Titanium dioxide 3.9%

Purpose

Sunscreen

Uses

  • Helps prevent sunburn.Provides high protection against sunburnRetains SPF after 40 minutes of activity in the water

Warnings

For external use only.

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 or irritation develops and lasts.

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 before sun exposure and as needed

Other Information

  • Sun alert: Limiting sun exposure, waring protective clothing, and using sunscreen may reduce the risk of skin aging, skin cancer, and other harmful effects of the sun.

Inactive Ingredients

Aqua (water), dicaprylyl carbonate, c12-15 alkyl benzoate, vp/eicosene copolymer, triethanolamine, methyl methacrylate crosspolymer, dimethicone, cyclopentasiloxane, cetearyl alcohol, sorbitan stearate, glyceryl stearate, potassium cetyl phosphate, tocopheryl acetate, cyclohexasiloxane, silica, trimethylsiloxysilicate, phenoxyethanol, methicone, ceteareth-20, methylparaben, xanthan gum, mannitol, parfum (fragrance), propylparaben, butylparaben, ethylparaben, isobutylparaben, arginine, cyclodextrin, dextrin, faex extract (yeast extract), histidine hydrochloride (histidine hci), pisum sativum extract (pisum sativum (pea) extract), acetyltyrosine, disodium succinate, khaya senegalensis bark extract, nicotinamide adenine dinucleotide, pyridoxine hci, aspartic acid.

* Please review the disclaimer below.