NDC 60905-0001 Givenchy Photo Perfexion Fluid Foundation Spf 20 Perfect Ivory Tint 1

Titanium Dioxide, Octinoxate

NDC Product Code 60905-0001

NDC CODE: 60905-0001

Proprietary Name: Givenchy Photo Perfexion Fluid Foundation Spf 20 Perfect Ivory Tint 1 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: Titanium Dioxide, Octinoxate 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

  • 60905 - Lvmh Fragrance Brands

NDC 60905-0001-1

Package Description: 1 BOTTLE in 1 CARTON > 25 mL in 1 BOTTLE

NDC 60905-0001-2

Package Description: 10 mL in 1 BOTTLE

NDC Product Information

Givenchy Photo Perfexion Fluid Foundation Spf 20 Perfect Ivory Tint 1 with NDC 60905-0001 is a a human over the counter drug product labeled by Lvmh Fragrance Brands. The generic name of Givenchy Photo Perfexion Fluid Foundation Spf 20 Perfect Ivory Tint 1 is titanium dioxide, octinoxate. The product's dosage form is liquid and is administered via topical form.

Labeler Name: Lvmh Fragrance Brands

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

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.

Givenchy Photo Perfexion Fluid Foundation Spf 20 Perfect Ivory Tint 1 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.

  • TITANIUM DIOXIDE 31.6 mg/mL
  • OCTINOXATE 29.97 mg/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)
  • ISODECYL NEOPENTANOATE (UNII: W60VYE24XC)
  • PENTYLENE GLYCOL (UNII: 50C1307PZG)
  • BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
  • SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
  • CYCLOMETHICONE 6 (UNII: XHK3U310BA)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
  • SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
  • DIMETHICONE (UNII: 92RU3N3Y1O)
  • ALUMINUM OXIDE (UNII: LMI26O6933)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • SODIUM MYRISTOYL GLUTAMATE (UNII: AYU7QD893W)
  • HYALURONATE SODIUM (UNII: YSE9PPT4TH)
  • SODIUM CITRATE (UNII: 1Q73Q2JULR)
  • BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69)
  • CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
  • ARTEMISIA CAPILLARIS FLOWER (UNII: KG4724BPZG)
  • BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
  • POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
  • GERANIOL (UNII: L837108USY)
  • BIOTIN (UNII: 6SO6U10H04)
  • FERRIC OXIDE RED (UNII: 1K09F3G675)
  • FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
  • FERROSOFERRIC OXIDE (UNII: XM0M87F357)
  • MICA (UNII: V8A1AW0880)

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.

Product Labeler Information

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

Labeler Name: Lvmh Fragrance Brands
Labeler Code: 60905
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: 07-08-2012 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

End Marketing Date: 10-01-2021 What is the End Marketing Date?
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.

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.

Givenchy Photo Perfexion Fluid Foundation Spf 20 Perfect Ivory Tint 1 Product Label Images

Givenchy Photo Perfexion Fluid Foundation Spf 20 Perfect Ivory Tint 1 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:

TITAINIUM DIOXIDE:  3.16%      OCTINOXATE (ETHYLHEXYL METHOXYCINNAMATE): 2.997%

Purpose

Sunscreen

Other Ingredients:

AQUA (WATER), CYCLOPENTASILOXANE, PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE, ISODECYL NEOPENTANOATE, PENTYLENE GLYCOL, SACCHAROMYCES/XYLINUM BLACK TEA FERMENT, BUTYLENE GLYCOL, ACRYLATES COPOLYMER, SILICA, CYCLOHEXASILOXANE, ACRYLATES / DIMETHICONE COPOLYMER, BUTYLENE GLYCOL DICAPRYLATE / DICAPRATE, PHENOXYETHANOL, ALUMINUM HYDROXIDE, STEARIC ACID, SORBITAN SESQUIOLEATE, DIMETHICONE CROSSPOLYMER, ALUMINA, GLYCERIN, SODIUM MYRISTOYL GLUTAMATE, HYDROXYETHYLCELLULOSE, SODIUM HYALURONATE, LECITHIN, PARFUM (FRAGRANCE), DIMETHICONE, SODIUM CITRATE, BUTYLPHENYL METHYLPROPIONAL, CITRIC ACID, DISODIUM DISTYRYLBIPHENYL DISULFONATE, ARTEMISIA CAPILLARIS FLOWER EXTRACT, BHT, POTASSIUM SORBATE, GERANIOL, BIOTIN.  [+/- MAY CONTAIN : CI 77891 (TITANIUM DIOXIDE),


CI 77491 - CI 77492 - CI 77499 (IRON OXIDES), MICA].

Warning:

FOR EXTERNAL USE ONLY.  AVOID CONTACT WITH EYES.

Discontinue Use

IF SIGNS OF IRRITATION APPEAR

Directions For Use:

Apply with the fingertips and smooth over the skin, working outwards from the center of the face. For a flawless, elegant, velvety finish that lasts all day long, follow with the PRISME LIBRE powder. For a perfect mat finish, follow with the PRISME VISAGE compact powder.

Shake Bottle

Before each use to mix the formula.  Close bottle well after use.

* Please review the disclaimer below.