NDC 61957-3141 Forever Skin Glow 24h Wear Radiant Foundation Perfection And Hydration Concentrated Floral Skincare With Suncreen Broad Spectrum Spf 15 00
Octisalate, Titanium Dioxide Emulsion Topical

Product Information

What is NDC 61957-3141?

The NDC code 61957-3141 is assigned by the FDA to the product Forever Skin Glow 24h Wear Radiant Foundation Perfection And Hydration Concentrated Floral Skincare With Suncreen Broad Spectrum Spf 15 00 which is a human over the counter drug product labeled by Parfums Christian Dior. The generic name of Forever Skin Glow 24h Wear Radiant Foundation Perfection And Hydration Concentrated Floral Skincare With Suncreen Broad Spectrum Spf 15 00 is octisalate, titanium dioxide. The product's dosage form is emulsion and is administered via topical form. The product is distributed in 2 packages with assigned NDC codes 61957-3141-0 30 ml in 1 bottle , 61957-3141-1 20 ml in 1 bottle . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information, RxNorm crosswalk and the complete product label.

NDC Product Code61957-3141
Proprietary Name 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.		Forever Skin Glow 24h Wear Radiant Foundation Perfection And Hydration Concentrated Floral Skincare With Suncreen Broad Spectrum Spf 15 00
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.		Octisalate, Titanium Dioxide
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.		Human Otc Drug
Dosage FormEmulsion - A dosage form consisting of a two-phase system comprised of at least two immiscible liquids1, one of which is dispersed as droplets (internal or dispersed phase) within the other liquid (external or continuous phase), generally stabilized with one or more emulsifying agents. (Note: Emulsion is used as a dosage form term unless a more specific term is applicable, e.g. cream, lotion, ointment.)
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.		Parfums Christian Dior
Labeler Code61957
FDA Application Number 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.		part352
Marketing Category 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.		OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
Start Marketing Date What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.		01-01-2022
Listing Expiration Date 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.		12-31-2023
Exclude Flag 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". 		N
NDC Code Structure

What are the uses for Forever Skin Glow 24h Wear Radiant Foundation Perfection And Hydration Concentrated Floral Skincare With Suncreen Broad Spectrum Spf 15 00?


Product Packages

NDC Code 61957-3141-0

Package Description: 30 mL in 1 BOTTLE

NDC Code 61957-3141-1

Package Description: 20 mL in 1 BOTTLE

Product Details

What are Forever Skin Glow 24h Wear Radiant Foundation Perfection And Hydration Concentrated Floral Skincare With Suncreen Broad Spectrum Spf 15 00 Active Ingredients?

An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

Forever Skin Glow 24h Wear Radiant Foundation Perfection And Hydration Concentrated Floral Skincare With Suncreen Broad Spectrum Spf 15 00 Active Ingredients UNII Codes

Forever Skin Glow 24h Wear Radiant Foundation Perfection And Hydration Concentrated Floral Skincare With Suncreen Broad Spectrum Spf 15 00 Inactive Ingredients UNII Codes

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.

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Forever Skin Glow 24h Wear Radiant Foundation Perfection And Hydration Concentrated Floral Skincare With Suncreen Broad Spectrum Spf 15 00 Product Label

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Label Table of Contents



Drug Facts




Active Ingredients



Octinoxate 4.50 %

Titanium Dioxide 4.23 %


Purpose



Sunscreen


Uses



  • Helps prevent sunburn.
  • If used as directed with other sun protection measures ( see Directions), decreases the risk of skin cancer and early skin aging caused by the sun.

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 swallowed, get medical help or contact a Poison Control Center right away.


Directions



  • Apply liberally 15 minutes before sun exposure.
  • 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 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.
  • Children under 6 months of age: ask a doctor.

Other Information



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

Inactive Ingredients



AQUA (WATER) • ALCOHOL • METHYL TRIMETHICONE • ISODODECANE • PHENYL TRIMETHICONE • GLYCERIN • PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE • TRIMETHTHYL PENTAPHENYL TRISILOXANE • ACRYLATES/DIMETHICONE COPOLYMER DIMETHICONE • BUTYLENE GLYCOL • CETYL DIMETHICONE • DISTEARDIMONIUM HECTORITE • CELLULOSE • CETYL PEG/PPG-10/1 DIMETHICONE • SODIUM MYRISTOYL GLUTAMATE • PARFUM (FRAGRANCE) • PROPYLENE CARBONATE • CHLORPHENESIN • VP/VA COPOLYMER • ALUMINA • STEARIC ACID • ALUMINUM HYDROXIDE • HIBISCUS SABDARIFFA FLOWER EXTRACT • TROMETHAMINE • TOCOPHEROL • TROPAEOLUM MAJUS FLOWER/LEAF/STEM EXTRACT • HEXADECENE • HYDROLYZED VIOLA TRICOLOR EXTRACT • 1,2-HEXANEDIOL • CAPRYLYL GLYCOL • IRIS FLORENTINA ROOT EXTRACT • SODIUM BENZOATE • POTASSIUM SORBATE • PENTAERYTHRITYL TETRA DI-BUTYL HYDROXYHYDROCINNAMATE.

[MAY CONTAIN : CI 77491, CI 77492, CI 77499 (IRON OXIDES), CI 77891 (TITANIUM DIOXIDE)].

N° 15857/Z


Package Labeling:30Ml



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Package Labeling:20Ml



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