NDC 14141-682 Lbel Effet Parfait Signs Of Age Appearance Minimizer Foundation Spf 20 Fm Claire 2 - Beige

Octinoxate And Titanium Dioxide

NDC Product Code 14141-682

NDC CODE: 14141-682

Proprietary Name: Lbel Effet Parfait Signs Of Age Appearance Minimizer Foundation Spf 20 Fm Claire 2 - Beige 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.

Non-Proprietary Name: Octinoxate And Titanium Dioxide What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

  • 14141 - Bel Star S.a. (colombia)
    • 14141-682 - Lbel Effet Parfait Signs Of Age Appearance Minimizer Foundation Spf 20 Fm

NDC 14141-682-02

Package Description: 1 BOTTLE in 1 BOX > 30 mL in 1 BOTTLE (14141-682-01)

NDC Product Information

Lbel Effet Parfait Signs Of Age Appearance Minimizer Foundation Spf 20 Fm Claire 2 - Beige with NDC 14141-682 is a a human over the counter drug product labeled by Bel Star S.a. (colombia). The generic name of Lbel Effet Parfait Signs Of Age Appearance Minimizer Foundation Spf 20 Fm Claire 2 - Beige is octinoxate and titanium dioxide. The product's dosage form is lotion and is administered via topical form.

Labeler Name: Bel Star S.a. (colombia)

Dosage Form: Lotion - An emulsion, liquid1 dosage form. This dosage form is generally for external application to the skin.2

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Lbel Effet Parfait Signs Of Age Appearance Minimizer Foundation Spf 20 Fm Claire 2 - Beige Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • OCTINOXATE .07 g/mL
  • TITANIUM DIOXIDE .0244 g/mL

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)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • COFFEE BEAN (UNII: JFH385Y744)
  • PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)
  • ALUMINUM OXIDE (UNII: LMI26O6933)
  • BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
  • OCTYLDODECANOL (UNII: 461N1O614Y)
  • CAPRYLYL GLYCOL (UNII: 00YIU5438U)
  • .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
  • CHLORPHENESIN (UNII: I670DAL4SZ)
  • BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
  • BENZYL ALCOHOL (UNII: LKG8494WBH)
  • POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
  • CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
  • POLYSORBATE 20 (UNII: 7T1F30V5YH)
  • PALMITOYL TRIPEPTIDE-1 (UNII: RV743D216M)
  • PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R)
  • FERRIC OXIDE RED (UNII: 1K09F3G675)
  • TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
  • HYDROGEN DIMETHICONE (13 CST) (UNII: 4QGR4P2YOI)
  • 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)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • COFFEE BEAN (UNII: JFH385Y744)
  • PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)
  • ALUMINUM OXIDE (UNII: LMI26O6933)
  • BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
  • OCTYLDODECANOL (UNII: 461N1O614Y)
  • CAPRYLYL GLYCOL (UNII: 00YIU5438U)
  • .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
  • CHLORPHENESIN (UNII: I670DAL4SZ)
  • BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
  • BENZYL ALCOHOL (UNII: LKG8494WBH)
  • POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
  • CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
  • POLYSORBATE 20 (UNII: 7T1F30V5YH)
  • PALMITOYL TRIPEPTIDE-1 (UNII: RV743D216M)
  • PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R)
  • FERRIC OXIDE RED (UNII: 1K09F3G675)
  • TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
  • HYDROGEN DIMETHICONE (13 CST) (UNII: 4QGR4P2YOI)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

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

Labeler Name: Bel Star S.a. (colombia)
Labeler Code: 14141
FDA Application Number: part352 What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

Marketing Category: OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph. What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 12-02-2019 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: N 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Lbel Effet Parfait Signs Of Age Appearance Minimizer Foundation Spf 20 Fm Claire 2 - Beige 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. For external use only.

Dist. by Ventura Corp, Ltd., San Juan, Puerto Rico 00926.

Otc - Purpose

Active IngredientsPurposeOCTINOXATE 7.00%,SunscreenTITANIUM DIOXIDE 2.44%Sunscreen

Uses

  • Helps prevent sunburn

Otc - Do Not Use

  • Do not use on damage 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 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 doctor.Reapply at least every 2 hours.Use a water resistant sunscreen if swimming or sweating.

Other Information

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

Inactive Ingredients

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, HYDROXYACETOPHENONE, PHENOXYETHANOL, COFFEA ARABICA (COFFEE) SEEDCAKE EXTRACT, PEG/PPG-18/18 DIMETHICONE, ALUMINA, BUTYLENE GLYCOL, OCTYLDODECANOL, CAPRYLYL GLYCOL, TOCOPHERYL ACETATE, CHLORPHENESIN, METHICONE, BHT, MICROCRYSTALLINE WAX, BENZYL ALCOHOL, PETROLATUM, PHOSPHOLIPIDS, POTASSIUM SORBATE, CARBOMER, CHOLESTEROL, POLYSORBATE 20, EUPHORBIA CERIFERA (CANDELILLA) WAX, BEESWAX, CETEARYL ALCOHOL, CETEARYL GLUCOSIDE, COPERNICIA CERIFERA (CARNAUBA) WAX, POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE, GLYCOSPHINGOLIPIDS, PALMITOYL TRIPEPTIDE-1, PALMITOYL TETRAPEPTIDE-7.MAY CONTAIN:TITANIUM DIOXIDE, IRON OXIDES, TRIETHOXYCAPRYLYLSILANE.

* Please review the disclaimer below.