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 product labeled by Temmentec Ag. 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)
  • 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.