NDC 68026-808 Skin Caviar Essence In Foundation Broad Spectrum Spf 25 Sunscreen Mocha

Avobenzone, Octinoxate, Octocrylene

NDC Product Code 68026-808

NDC Code: 68026-808

Proprietary Name: Skin Caviar Essence In Foundation Broad Spectrum Spf 25 Sunscreen Mocha Additional informationCallout TooltipWhat 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: Avobenzone, Octinoxate, Octocrylene Additional informationCallout TooltipWhat 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.


Code Structure
  • 68026 - La Prairie, Inc.
    • 68026-808 - Skin Caviar Essence In Foundation Broad Spectrum Spf 25 Sunscreen Mocha

NDC 68026-808-30

Package Description: 2 CONTAINER in 1 CARTON > 15 mL in 1 CONTAINER

NDC Product Information

Skin Caviar Essence In Foundation Broad Spectrum Spf 25 Sunscreen Mocha with NDC 68026-808 is a a human over the counter drug product labeled by La Prairie, Inc.. The generic name of Skin Caviar Essence In Foundation Broad Spectrum Spf 25 Sunscreen Mocha is avobenzone, octinoxate, octocrylene. The product's dosage form is lotion and is administered via topical form.

Labeler Name: La Prairie, Inc.

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 Additional informationCallout TooltipWhat 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.


Skin Caviar Essence In Foundation Broad Spectrum Spf 25 Sunscreen Mocha Active Ingredient(s)

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

  • AVOBENZONE 20 mg/mL
  • OCTINOXATE 30 mg/mL
  • OCTOCRYLENE 40 mg/mL

Inactive Ingredient(s)

Additional informationCallout TooltipAbout 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.

  • CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
  • WATER (UNII: 059QF0KO0R)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
  • DIMETHICONE (UNII: 92RU3N3Y1O)
  • MYRISTYL LACTATE (UNII: 1D822OC34X)
  • HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)
  • POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
  • BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
  • LARICIFOMES OFFICINALIS FRUITING BODY (UNII: 7IFM8431X3)
  • DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6)
  • ACRYLIC ACID/ETHYLENE COPOLYMER (600 MPA.S) (UNII: 1PEZ3NLY6I)
  • ASIAN GINSENG (UNII: CUQ3A77YXI)
  • EQUISETUM ARVENSE BRANCH (UNII: 1L0VKZ185E)
  • CAVIAR, UNSPECIFIED (UNII: 020K6HLU0O)
  • TETRAPEPTIDE-3 (UNII: 90AX5T9G36)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • CHONDRUS CRISPUS CARRAGEENAN (UNII: UE856F2T78)
  • POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
  • LACTOBACILLUS REUTERI (UNII: 9913I24QEE)
  • .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
  • SOYBEAN OIL (UNII: 241ATL177A)
  • DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
  • LACTIC ACID, UNSPECIFIED FORM (UNII: 33X04XA5AT)
  • ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
  • HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
  • EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
  • SODIUM LAUROYL GLUTAMATE (UNII: NCX1UU2D33)
  • PHYTATE SODIUM (UNII: 88496G1ERL)
  • TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
  • PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS)
  • LYSINE (UNII: K3Z4F929H6)
  • MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
  • SODIUM OLEATE (UNII: 399SL044HN)
  • SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W)
  • ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
  • ALCOHOL (UNII: 3K9958V90M)
  • SACCHAROMYCES CEREVISIAE (UNII: 978D8U419H)
  • SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
  • SODIUM SALICYLATE (UNII: WIQ1H85SYP)
  • SODIUM CHLORIDE (UNII: 451W47IQ8X)
  • BENZYL ALCOHOL (UNII: LKG8494WBH)
  • LINALOOL, (+/-)- (UNII: D81QY6I88E)
  • ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)
  • GERANIOL (UNII: L837108USY)
  • .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
  • BENZYL SALICYLATE (UNII: WAO5MNK9TU)
  • SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
  • SODIUM BENZOATE (UNII: OJ245FE5EU)
  • POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)

Administration Route(s)

Additional informationCallout TooltipWhat 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.

Product Labeler Information

Additional informationCallout TooltipWhat is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: La Prairie, Inc.
Labeler Code: 68026
FDA Application Number: part352 Additional informationCallout TooltipWhat 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 NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final. Additional informationCallout TooltipWhat 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: 02-01-2019 Additional informationCallout TooltipWhat 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 Additional informationCallout TooltipWhat 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 Additional informationCallout TooltipWhat 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.

Skin Caviar Essence In Foundation Broad Spectrum Spf 25 Sunscreen Mocha Product Label Images

Skin Caviar Essence In Foundation Broad Spectrum Spf 25 Sunscreen Mocha 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 2.0 %Octinoxate 3.0 %Octocrylene 4.0 %

Purpose

Sunscreen

Uses

• helps prevent sunburn

Warnings

For external use only.

Do Not Use

On damaged or broken skin.

When Using This Product

Keep out of eyes. Rinse with water to remove.

Stop Use And Ask A Doctor

If rash occurs.

Keep Out Of Reach Of Children.

If product is swallowed, get medical help or contact a Poison

Directions

• apply daily after cleansing and toning


• smooth over face & throat


• apply liberally 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





Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including:


• Limit time in the sun, especially from 10 a.m. – 2 p.m.


• Wear long-sleeve shirts, pants, hats, and sunglasses

Inactive Ingredients

Caviar Water, Cyclopentasiloxane, Cetyl PEG/PPG-10/1 Dimethicone, Water (Aqua), Glycerin, C12-15 Alkyl Benzoate, Dimethicone, Myristyl Lactate, HDI/Trimethylol Hexyllactone Crosspolymer, Polyglyceryl-4 Isostearate, Butylene Glycol, Trimethylsiloxysilicate, Fomes Officinalis (Mushroom) Extract, Dimethicone Crosspolymer, Ethylene/Acrylic Acid Copolymer, Glycoproteins*, Panax Ginseng Root Extract*, Equisetum Arvense Extract*, Caviar Extract, Lithothamnium Calcarum Extract, Tetrapeptide-3, Propylene Glycol, Chondrus Crispus Extract, PEG-40 Hydrogenated Castor Oil, Lactobacillus Ferment, Tocopheryl Acetate, Glycine Soja (Soybean) Oil, Disteardimonium Hectorite, Synthetic Fluorphlogopite, Lactic Acid, Aluminum Hydroxide, Hydrogenated Lecithin, Disodium EDTA, Sodium Lauroyl Glutamate, Sodium Phytate, Triethoxycaprylylsilane, Pentaerythrityl Tetra-Di-T-Butyl Hydroxyhydrocinnamate, Lysine, Magnesium Chloride, Sodium Oleate, Silica Dimethyl Silylate, Ethylhexylglycerin, Alcohol, Saccharomyces Cerevisiae Extract, Silica, Sodium Salicylate, Sodium Chloride, Fragrance (Parfum), Benzyl Alcohol, Linalool, Limonene, Alpha-Isomethyl Ionone, Geraniol, Citronellol, Benzyl Salicylate, Sodium Dehydroacetate, Sodium Benzoate, Potassium Sorbate, PhenoxyethanolMay Contain [+/- : Titanium Dioxide (CI 77891), Iron Oxides (CI 77491), Iron Oxides (CI 77492), Iron Oxides (CI 77499)] i72 * New patent pending for La Prairie’s exclusive Cellular Complex in addition to US Patent 5,840,309

Other Information

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

* Please review the disclaimer below.

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