NDC 69000-010 Time Frame Future Resist Foundation Broad Spectrum Spf 20 Delilah Cosmetics

NDC Product Code 69000-010

NDC CODE: 69000-010

Proprietary Name: Time Frame Future Resist Foundation Broad Spectrum Spf 20 Delilah Cosmetics 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: 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

  • 69000 - Delilah Cosmetics
    • 69000-010 - Time Frame Future Resist Foundation Broad Spectrum Spf 20

NDC 69000-010-02

Package Description: 1 TUBE in 1 CARTON > 38 mL in 1 TUBE (69000-010-01)

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

NDC Product Information

Time Frame Future Resist Foundation Broad Spectrum Spf 20 Delilah Cosmetics with NDC 69000-010 is a product labeled by Delilah Cosmetics. The generic name of Time Frame Future Resist Foundation Broad Spectrum Spf 20 Delilah Cosmetics is . The product's dosage form is and is administered via form.

Labeler Name: Delilah Cosmetics

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 (UNII: NMQ347994Z)
  • ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)
  • CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
  • PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
  • C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
  • DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
  • SODIUM CHLORIDE (UNII: 451W47IQ8X)
  • ALUMINUM OXIDE (UNII: LMI26O6933)
  • SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
  • METHICONE (20 CST) (UNII: 6777U11MKT)
  • TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
  • MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
  • TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)
  • DIMETHICONE (UNII: 92RU3N3Y1O)
  • TROPOLONE (UNII: 7L6DL16P1T)
  • FERRIC OXIDE RED (UNII: 1K09F3G675)
  • FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
  • FERROSOFERRIC OXIDE (UNII: XM0M87F357)

Product Labeler Information

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

Labeler Name: Delilah Cosmetics
Labeler Code: 69000
Start Marketing Date: 10-07-2014 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: 12-31-2019 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.

Time Frame Future Resist Foundation Broad Spectrum Spf 20 Delilah Cosmetics Product Label Images

Time Frame Future Resist Foundation Broad Spectrum Spf 20 Delilah Cosmetics 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           PurposeTitanium Dioxide 5%       Sunscreen

Otc - Purpose

UsesHelps prevent SunburnIf used as directed with other sun protection measures (see Directions), decrease the risk of skin cancer and early skin aging caused by the sun.

Otc - Keep Out Of Reach Of Children

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

Indications & Usage

Stop use and ask a dcotor if rash occurs.

Warnings

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

Dosage & Administration

DirectionsApply foundation liberally to clean face for Broad Spectrum protection. Reapply as needed.This is not a primary Sunscreen. For further protection by a primary Sunscreen follow directions below.Apply primary Sunscreen liberally 15 minutes before sun exposureReapply at least every 2 hours.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 15 or higher and other sun protection measures including:Limit time in the sun, especially 10 a.m. - 2 p.m.Wear long-sleeve shirts, pants, hats, and sunglassesChildren under 6 months ask doctor

Inactive Ingredient

Inactive Ingredients: Water/Aqua, Cyclomethicone, Butylene Glycol, Isononyl Isononoate, Behenyl Dimethicone, Cetyl PEG/PPG-10/1 Dimethicone, Phenyl Trimethicone, C12-15 Alkyl Benzoate, Disteardimonium Hectorite, Glcyeryl Ethylhexanoate/Stearate/Adipate, Phenoxyethanol, Sucrose Acetyl Isobutyrate, Tocopheryl Acetate, Sodium Chloride, Lauryl PEG-8 Dimethicone, Alumina, Sodium Dehydroacetate, Methicone, Triethoxycaprylylsilane, Caprylic/Capric Triglyceride, Trisodium Ethylenediamine Dissucinate, Dimethicone, Tropolone, Tripeptide-3, Hexapeptide-4, (May contain (+/-) CI 77891 (Titanium Dioxide), CI 77491 (iron oxides), CI 77492 (Iron Oxides), CI 77499 (Iron Oxides).

* Please review the disclaimer below.