NDC 70186-603 Light Wonder Your Light, Dream Skin Foundation Sunscreen Broad Spectrum Spf 15

Octinoxate And Titanium Dioxide

NDC Product Code 70186-603

NDC Code: 70186-603

Proprietary Name: Light Wonder Your Light, Dream Skin Foundation Sunscreen Broad Spectrum Spf 15 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: Octinoxate And Titanium Dioxide 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

  • 70186 - Charlotte Tilbury Beauty Ltd.
    • 70186-603 - Light Wonder Your Light, Dream Skin Foundation Sunscreen Broad Spectrum Spf 15

NDC 70186-603-01

Package Description: 1 TUBE in 1 CARTON > 40 mL in 1 TUBE

NDC Product Information

Light Wonder Your Light, Dream Skin Foundation Sunscreen Broad Spectrum Spf 15 with NDC 70186-603 is a a human over the counter drug product labeled by Charlotte Tilbury Beauty Ltd.. The generic name of Light Wonder Your Light, Dream Skin Foundation Sunscreen Broad Spectrum Spf 15 is octinoxate and titanium dioxide. The product's dosage form is suspension and is administered via topical form.

Labeler Name: Charlotte Tilbury Beauty Ltd.

Dosage Form: Suspension - A liquid1 dosage form that contains solid particles dispersed in a liquid vehicle.

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.

Light Wonder Your Light, Dream Skin Foundation Sunscreen Broad Spectrum Spf 15 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.

  • OCTINOXATE 1.76 g/40mL
  • TITANIUM DIOXIDE 1 g/40mL

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.

  • CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
  • WATER (UNII: 059QF0KO0R)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)
  • PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)
  • SODIUM CHLORIDE (UNII: 451W47IQ8X)
  • CYCLOMETHICONE 6 (UNII: XHK3U310BA)
  • DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
  • CETEARYL ETHYLHEXANOATE (UNII: 9M64UO4C25)
  • SQUALANE (UNII: GW89575KF9)
  • DIMETHICONE (UNII: 92RU3N3Y1O)
  • DISODIUM COCOYL GLUTAMATE (UNII: MBK0CP8F5A)
  • METHYLPARABEN (UNII: A2I8C7HI9T)
  • POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
  • ISOPROPYL TITANIUM TRIISOSTEARATE (UNII: 949E3KBJ1I)
  • PROPYLPARABEN (UNII: Z8IX2SC1OH)
  • SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
  • SOY STEROL (UNII: PL360EPO9J)
  • SODIUM COCOYL GLUTAMATE (UNII: BMT4RCZ3HG)
  • ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
  • LAURETH-4 (UNII: 6HQ855798J)
  • PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS)
  • BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
  • MICA (UNII: V8A1AW0880)
  • FERRIC OXIDE RED (UNII: 1K09F3G675)
  • CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
  • WATER (UNII: 059QF0KO0R)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)
  • PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)
  • SODIUM CHLORIDE (UNII: 451W47IQ8X)
  • CYCLOMETHICONE 6 (UNII: XHK3U310BA)
  • DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
  • CETEARYL ETHYLHEXANOATE (UNII: 9M64UO4C25)
  • SQUALANE (UNII: GW89575KF9)
  • DIMETHICONE (UNII: 92RU3N3Y1O)
  • DISODIUM COCOYL GLUTAMATE (UNII: MBK0CP8F5A)
  • METHYLPARABEN (UNII: A2I8C7HI9T)
  • POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
  • ISOPROPYL TITANIUM TRIISOSTEARATE (UNII: 949E3KBJ1I)
  • PROPYLPARABEN (UNII: Z8IX2SC1OH)
  • SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
  • SOY STEROL (UNII: PL360EPO9J)
  • SODIUM COCOYL GLUTAMATE (UNII: BMT4RCZ3HG)
  • ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
  • LAURETH-4 (UNII: 6HQ855798J)
  • PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS)
  • BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
  • MICA (UNII: V8A1AW0880)
  • FERRIC OXIDE RED (UNII: 1K09F3G675)
  • CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
  • WATER (UNII: 059QF0KO0R)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)
  • PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)
  • SODIUM CHLORIDE (UNII: 451W47IQ8X)
  • CYCLOMETHICONE 6 (UNII: XHK3U310BA)
  • DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
  • CETEARYL ETHYLHEXANOATE (UNII: 9M64UO4C25)
  • SQUALANE (UNII: GW89575KF9)
  • DIMETHICONE (UNII: 92RU3N3Y1O)
  • DISODIUM COCOYL GLUTAMATE (UNII: MBK0CP8F5A)
  • METHYLPARABEN (UNII: A2I8C7HI9T)
  • POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
  • ISOPROPYL TITANIUM TRIISOSTEARATE (UNII: 949E3KBJ1I)
  • PROPYLPARABEN (UNII: Z8IX2SC1OH)
  • SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
  • SOY STEROL (UNII: PL360EPO9J)
  • SODIUM COCOYL GLUTAMATE (UNII: BMT4RCZ3HG)
  • ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
  • LAURETH-4 (UNII: 6HQ855798J)
  • PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS)
  • BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
  • MICA (UNII: V8A1AW0880)
  • FERRIC OXIDE RED (UNII: 1K09F3G675)

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: Charlotte Tilbury Beauty Ltd.
Labeler Code: 70186
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 NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final. 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: 06-01-2019 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: 12-31-2020 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: 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.

Light Wonder Your Light, Dream Skin Foundation Sunscreen Broad Spectrum Spf 15 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

Warnings And Precautions

Drug Facts

Otc - Purpose

Active Ingredients         PurposeOctinoxate 3.99%             SunscreenTitanium Dioxide 2.28%    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

Otc - Do Not Use

Do not use on damaged or broken skin

Otc - When Using

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

Otc - Stop Use

Stop use and ask a doctor if rash occurs.

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.

Directions

• shake before use• Apply liberally and evenly 15 minutes before sun exposure• Children under 6 months of age: Ask a doctor• Sun Protection Measure. 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 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-sleeved shirts, pants, hats, and sunglasses- Reapply at least every 2 hours and immediately after towel drying- Use a water-resistant sunscreen if swimming or sweating

Inactive Ingredients

Cyclopentasiloxane, Water, Hydrogenated Didodecene, Glycerin, Sorbitan Isostearate, PEG/PPG-18/18 Dimethicone, Sodium Chloride, Cyclohexasiloxane, Aluminum/Magnesium Hydroxide Stearate, Dimethicone/Vinyl Dimethicone Crosspolymer, Cetearyl Ethylhexanoate, Squalane, Dimethicone, Disodium Cocoyl Glutamate, Methylparaben, Potassium Sorbate, Isopropyl Titanium Triisostearate, Propylparaben, Silica, Fragrance, Glycine Soja (Soybean) Sterols, Sodium Cocoyl Glutamate, Aluminum Hydroxide, Laureth-4, Pentaerythrityl Tetra-Di-t-Butyl Hydroxyhydrocinnamate, BHT. May Contain: Mica, Titanium Dioxide, Iron Oxides.

Other Information

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

* Please review the disclaimer below.

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