NDC 68807-316 Anti-aging Day Broad Spectrum Spf 30 La Prairie Group Ag

NDC Product Code 68807-316

NDC 68807-316-11

Package Description: 78.4 kg in 1 DRUM

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

NDC Product Information

Anti-aging Day Broad Spectrum Spf 30 La Prairie Group Ag with NDC 68807-316 is a product labeled by Temmentec Ag. The generic name of Anti-aging Day Broad Spectrum Spf 30 La Prairie Group Ag is . The product's dosage form is and is administered via form.

Labeler Name: Temmentec Ag

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)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
  • STEARETH-21 (UNII: 53J3F32P58)
  • DOCOSANOL (UNII: 9G1OE216XY)
  • BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
  • ASIAN GINSENG (UNII: CUQ3A77YXI)
  • HYALURONATE SODIUM (UNII: YSE9PPT4TH)
  • SALICORNIA EUROPAEA (UNII: 6ADL50JAKW)
  • SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
  • .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
  • RESVERATROL (UNII: Q369O8926L)
  • TREHALOSE (UNII: B8WCK70T7I)
  • UREA (UNII: 8W8T17847W)
  • LARIX SIBIRICA WOOD (UNII: KSC3PGF73L)
  • CARNOSINE (UNII: 8HO6PVN24W)
  • EDETATE DISODIUM (UNII: 7FLD91C86K)
  • MYROTHAMNUS FLABELLIFOLIA LEAF (UNII: 6Y9E0R40J5)
  • SODIUM HYDROXIDE (UNII: 55X04QC32I)
  • GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
  • CHLORELLA VULGARIS (UNII: RYQ4R60M02)
  • SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
  • PANTHENOL (UNII: WV9CM0O67Z)
  • POLYQUATERNIUM-51 (2-METHACRYLOYLOXYETHYL PHOSPHORYLCHOLINE/N-BUTYL METHACRYLATE; 3:7) (UNII: EL9825H96J)
  • SOYBEAN OIL (UNII: 241ATL177A)
  • PEG-100 STEARATE (UNII: YD01N1999R)
  • HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
  • ALLANTOIN (UNII: 344S277G0Z)
  • HYDROXYETHYL BEHENAMIDOPROPYL DIMONIUM CHLORIDE (UNII: 9CO8OUL4TH)
  • C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
  • MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
  • POLYSORBATE 80 (UNII: 6OZP39ZG8H)
  • SODIUM OLEATE (UNII: 399SL044HN)
  • LAURETH-7 (UNII: Z95S6G8201)
  • CETYL DIMETHICONE 25 (UNII: U4AS1BW4ZB)
  • CAPRYLYL GLYCOL (UNII: 00YIU5438U)
  • STEARETH-2 (UNII: V56DFE46J5)
  • POLYACRYLAMIDE (1500 MW) (UNII: 5D6TC4BRWV)
  • CARBOMER 934 (UNII: Z135WT9208)
  • SYNTHETIC WAX (1800 MW) (UNII: 248P1AUJ90)
  • ALCOHOL (UNII: 3K9958V90M)
  • LINALOOL, (+/-)- (UNII: D81QY6I88E)
  • .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
  • HYDROXYCITRONELLAL (UNII: 8SQ0VA4YUR)
  • ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)
  • GERANIOL (UNII: L837108USY)
  • .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
  • BENZYL BENZOATE (UNII: N863NB338G)
  • BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69)
  • PSEUDEVERNIA FURFURACEA (UNII: 49ZMN09Q0K)
  • EUGENOL (UNII: 3T8H1794QW)
  • BENZYL SALICYLATE (UNII: WAO5MNK9TU)
  • LIMONENE, (+)- (UNII: GFD7C86Q1W)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • SORBIC ACID (UNII: X045WJ989B)
  • CHLORPHENESIN (UNII: I670DAL4SZ)
  • METHYLPARABEN (UNII: A2I8C7HI9T)
  • BENZOIC ACID (UNII: 8SKN0B0MIM)
  • FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
  • FD&C RED NO. 4 (UNII: X3W0AM1JLX)

Product Labeler Information

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

Labeler Name: Temmentec Ag
Labeler Code: 68807
Start Marketing Date: 01-16-2013 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: 12-31-2018 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.

Anti-aging Day Broad Spectrum Spf 30 La Prairie Group Ag Product Label Images

Anti-aging Day Broad Spectrum Spf 30 La Prairie Group Ag 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 purposeAvobenzone 3.0% SunscreenOctinoxate 7.5% SunscreenOctisalate 5.0% SunscreenOctocrylene 2.5% Sunscreen

Otc - Purpose

  • Useshelps prevent sunburn

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

Indications & Usage

Stop use and ask a doctor if rash occurs.

Warnings

WarningsFor external use only Do not use on damaged or broken skinWhen using this product keep out of eyes. Rinse with water to remove.

Dosage & Administration

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 sweatingSun Protection Measures. Spending time in the sun increases your risk of skin cancerand early skin aging. To decrease this risk, regularly use a sunscreen with a Broad SpectrumSPF 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 Ingredient

Water (Aqua), C12-15 Alkyl Ethylhexanoate, Glycerin, Dimethicone/Vinyl DimethiconeCrosspolymer, Polyglyceryl-3 Methylglucose Distearate, Helianthus Annuus (Sunflower) Seed Oil Unsaponifiables, Steareth-21, Behenyl Alcohol, Butylene Glycol, Glycoproteins, Panax Ginseng Root Extract, Equisetum Arvense (Horsetail) Extract, Sodium Hyaluronate, Caprooyl Tetrapeptide-3, Salicornia Herbacea Extract, Sodium PCA, Tocopheryl Acetate, Resveratrol, Acetyl Decapeptide-3, Trehalose, Urea, Larix Sibirica Wood Extract, Palmitoyl Tripeptide-8, Carnosine, Potato Starch Modified, Disodium EDTA, Myrothamnus Flabellifolia Leaf/Stem Extract, Kefiran, Sodium Hydroxide, Glyceryl Stearate, Chlorella Vulgaris Extract, Silica, Panthenol, Polyquaternium-51, Glycine Soja (Soybean) Oil, PEG-100 Stearate, Hydrogenated Lecithin, Allantoin, Hydroxyethyl Behenamidopropyl Dimonium Chloride, C13-14 Isoparaffin, Dextran, Caprylic/Capric Triglyceride, Polysorbate 80, Sodium Oleate, Laureth-7, Cetyl Dimethicone, Caprylyl Glycol, Polyquaternium-67, Steareth-2, Polyacrylamide, Carbomer, Synthetic Wax, Alcohol, Fragrance (Parfum), Linalool, Hexyl Cinnamal, Hydroxycitronellal, Alpha-Isomethyl Ionone, Geraniol, Citronellol, Benzyl Benzoate, Butylphenyl Methylpropional, Evernia Furfuracea (Treemoss) Extract, Eugenol, Benzyl Salicylate, Limonene, Phenoxyethanol, Sorbic Acid, Chlorphenesin, Methylparaben, Benzoic Acid, Yellow 5 (CI 19140), Red 4 (CI 14700)

* Please review the disclaimer below.