NDC 42627-207 Veil Fluid Makeup Beige Spf 15

Octinoxate, Octisalate, Oxybenzone

NDC Product Code 42627-207

NDC CODE: 42627-207

Proprietary Name: Veil Fluid Makeup Beige 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, Octisalate, Oxybenzone 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

  • 42627 - Kingdom Animalia, Llc. Dba Hourglass Cosmetics

NDC 42627-207-02

Package Description: 1 TUBE in 1 CARTON > 50 mL in 1 TUBE (42627-207-01)

NDC Product Information

Veil Fluid Makeup Beige Spf 15 with NDC 42627-207 is a a human over the counter drug product labeled by Kingdom Animalia, Llc. Dba Hourglass Cosmetics. The generic name of Veil Fluid Makeup Beige Spf 15 is octinoxate, octisalate, oxybenzone. The product's dosage form is emulsion and is administered via topical form.

Labeler Name: Kingdom Animalia, Llc. Dba Hourglass Cosmetics

Dosage Form: Emulsion - 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.)

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.

Veil Fluid Makeup Beige 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 7.5 g/100mL
  • OCTISALATE 4 g/100mL
  • OXYBENZONE 3 g/100mL

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)
  • MAGNESIUM SULFATE (UNII: DE08037SAB)
  • PALMITOYL TRIPEPTIDE-5 (UNII: 2A3916MQHO)
  • HYDROLYZED WHEAT PROTEIN (ENZYMATIC, 3000 MW) (UNII: J2S07SB0YL)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
  • BIOTIN (UNII: 6SO6U10H04)
  • EDETATE TRISODIUM (UNII: 420IP921MB)
  • SODIUM BENZOATE (UNII: OJ245FE5EU)
  • POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
  • CETYL PEG/PPG-10/1 DIMETHICONE (HLB 5) (UNII: 035JKJ76MT)
  • HEXYL LAURATE (UNII: 4CG9F9W01Q)
  • .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
  • GLYCERYL DIBEHENATE (UNII: R8WTH25YS2)
  • TRIBEHENIN (UNII: 8OC9U7TQZ0)
  • ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
  • ISODODECANE (UNII: A8289P68Y2)
  • QUATERNIUM-91 (UNII: 00J8H295NB)
  • PROPYLENE CARBONATE (UNII: 8D08K3S51E)
  • CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
  • DIMETHICONE (UNII: 92RU3N3Y1O)
  • CETEARYL ETHYLHEXANOATE (UNII: 9M64UO4C25)
  • PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
  • SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
  • PENTAERYTHRITYL TETRAISOSTEARATE (UNII: 9D7IK5483F)
  • ISOEICOSANE (UNII: AR294KAG3T)
  • TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
  • FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
  • FERRIC OXIDE RED (UNII: 1K09F3G675)
  • FERROSOFERRIC OXIDE (UNII: XM0M87F357)

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: Kingdom Animalia, Llc. Dba Hourglass Cosmetics
Labeler Code: 42627
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: 06-01-2012 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: 03-31-2021 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.

Veil Fluid Makeup Beige Spf 15 Product Label Images

Veil Fluid Makeup Beige 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

Otc - Active Ingredient

Active Ingredients               PurposeOctinoxate  7.5%                          SunscreenOctisalate  4.0%                           SunscreenOxybenzone 3.0%                         Sunscreen

Otc - Purpose

Enter section text here

Indications & Usage

  • Useshelps prevent sunburnif used as directed with other sun protection measures (see Directions), decrease the risk of skin cancer and early skin aging cause by the sun.

Warnings

For external use only.

Otc - Do Not Use

Do not use on damage or broken skin.

Otc - When Using

When using this product keep out of eyes.  If contact occurs, rinse thoroughly with water.

Otc - Stop Use

Stop Use and ask a doctor if irritation or rash develops.

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.

Instructions For Use

  • DirectionsSHAKE WELL, and apply to moisturized or primed skin with fingertips or Hourglass Foundation Brush.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:  Ask a doctor.

Inactive Ingredient

Inactive Ingredients  CETEARYL ETHYLHEXANOATE, CETYL PEG/PPG 10/1 DIMETHICONE, CYCLOPENTASILOXANE, DIMETHICONE, ETHYLHEXYLGLYCERIN, GLYCERIN, GLYCERYL BEHENATE, GLYCERYL DIBEHENATE, HDI/TRIMETHYLOL HEXYLLACTONE CROSS-POLYMER, HEXYL LAURATE, HYDROLYZED WHEAT PROTEIN, HYDOXYPROPYL CYCLODEXTRIN, ISODODECANE, ISOEICOSANE, MACROCYSTIC PYRIFERA EXTRACT, MAGNESIUM SULFATE, PALMITOYL TRIPEPTIDE-38, PENTAERYTHRITYL TETRAISOSTEARATE, PHENOXYETHANOL, PHENYL TRIMETHICONE, POLYGLYCERYL-4 ISOSTEARATE, POTASSIUM SORBATE, PROPYLENE CARBONATE, PVP, QUATERNIUM-90 BENTONITE, SILICA, SODIUM BENZOATE, TOCOPHERYL ACETATE, TRIBEHENIN, TRIETHOXYLCAPRYLYLSILANE, WATER. MAY CONTAIN (+/-): IRON OXIDES (CI 77491), IRON OXIDES (CI 77492), IRON OXIDES (CI 77499), TITANIUM DIOXIDE (CI 77891).

Other Safety Information

Other Information Protect this product from excessive heat and direct sun.

Otc - Questions

Questions or comments?CALL TOLL FREE 855-201-4529

How Supplied

DIST. BY KINGDOM ANIMALIA, LLC.  VENICE, CA 90291  USAHOURGLASS COSMETICS, UK LTD, LONDON WC1D 3JAMADE IN USA   PRODUCT NOT TESTED ON ANIMALS

* Please review the disclaimer below.