NDC 59614-221 Sun Protection Emulsion Face La Prairie

  1. Labeler Index
  2. Juvena Gmbh
  3. NDC: 59614-221 Sun Protection Emulsion Face La Prairie

NDC Product Code 59614-221

NDC CODE: 59614-221

Proprietary Name: Sun Protection Emulsion Face La Prairie 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: 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

NDC 59614-221-02

Package Description: 1 BOTTLE in 1 BOX > 125 mL in 1 BOTTLE (59614-221-01)

NDC 59614-221-11

Package Description: .088 mL in 1 DRUM

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

NDC Product Information

Sun Protection Emulsion Face La Prairie with NDC 59614-221 is a product labeled by Juvena Gmbh. The generic name of Sun Protection Emulsion Face La Prairie is . The product's dosage form is and is administered via form.

Labeler Name: Juvena Gmbh

Dosage Form: -

Product Type: 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.

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.
  • HEXYLDECANOL (UNII: 151Z7P1317)
  • DIMETHICONE (UNII: 92RU3N3Y1O)
  • ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
  • STEARETH-21 (UNII: 53J3F32P58)
  • CETYL ALCOHOL (UNII: 936JST6JCN)
  • SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • STEARETH-2 (UNII: V56DFE46J5)
  • EDETATE DISODIUM (UNII: 7FLD91C86K)
  • SODIUM HYDROXIDE (UNII: 55X04QC32I)
  • SQUALANE (UNII: GW89575KF9)
  • POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
  • POLYSORBATE 60 (UNII: CAL22UVI4M)
  • MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
  • SODIUM LACTATE (UNII: TU7HW0W0QT)
  • CAPRYLYL GLYCOL (UNII: 00YIU5438U)
  • ALCOHOL (UNII: 3K9958V90M)
  • BENZYL ALCOHOL (UNII: LKG8494WBH)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • CHLORPHENESIN (UNII: I670DAL4SZ)
  • SODIUM BENZOATE (UNII: OJ245FE5EU)
  • METHYLPARABEN (UNII: A2I8C7HI9T)
  • ETHYLPARABEN (UNII: 14255EXE39)
  • PROPYLPARABEN (UNII: Z8IX2SC1OH)

Product Labeler Information

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

Labeler Name: Juvena Gmbh
Labeler Code: 59614
Start Marketing Date: 02-14-2011 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 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.

Sun Protection Emulsion Face La Prairie Product Label Images

Sun Protection Emulsion Face La Prairie 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

Otc - Active Ingredient

Active Ingredients            Purpose Avobenzone 3.0%            sunscreen Homosalate   10.0%         sunscreen Octisalate 2.6%                sunscreen octocrylene 2.4%              sunscreen Oxybenzone 5.0%            sunscreen

Otc - Purpose

- Helps prevent sunburn - for skin that burns easily -provides moderate protection against sunburn-higher SPF gives more sunburn protection

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. Do not use on infants under 6 months of age.

Indications & Usage

Stop use and ask a doctor if rash or irritation develops and lasts.

Warnings

When using this product keep out of eyes. rinse with water to remove.

Dosage & Administration

Apply daily after cleansing and toning .Smooth over face and throat.Apply evenly before sun exposure. Reapply as needed or after towel drying, swimming or perspiring.

Inactive Ingredient

Water (Aqua), Caprylyl Methicone, Hexyldecanol, Dimethicone, Polyglyceryl-3 Methylglucose Distearate, Undercrylene Dimethicone, Aluminum Starch Octenylsuccinate, Steareth-21, Octyldodecyl Olivate, Cetyl Alcohol, Silica, Glycerin, Glycoproteins, Panax Ginseng Root Extract*, Equisetum Arvense (Horsetail) Extract*, Sodium Hyaluronate, Corallina Officinalis Extract, Sea Water ( Maris Aqua), Algae Extract, Aloe Barbadensis Leaf Juice, Steareth-2, Ethylhexyl Glycerin, Disodium EDTA, Benzylidene Dimethoxydimethylindanone, sodium hydroxide, porphyra Umbilicalis Extract, Squalane, Carbomer, Potassium Sorbate, Hydroxyethyl acrylate/ Sodium Acryloyldimethyl Taurate Copolymer, Palmaria Pakmata Extract, Tocopheryl Acetate, Diethylhexyl Syringyldenemalonate, Pelvetia Canaliculata Extract, Polysorbate 60, Lecithin, Caprylic/ Capric Triglyceride, Sodium Lactate, Caprylyl Glycol, Alcohol, Benzyl Alcohol, Fragrance ( parfum), Phenoxyethanol, Chlorphenesin, Sodium Benzoate, Methylparaben, Ethylparaben, Propyparaben

* Please review the disclaimer below.