NDC 75936-164 Unseen Sunscreen Broad Spectrum Spf 40

Avobenzone, Homosalate, Octinoxate, Octisalate

NDC Product Code 75936-164

NDC 75936-164-02

Package Description: 1 PACKAGE in 1 CARTON > 50 mL in 1 PACKAGE (75936-164-01)

NDC 75936-164-03

Package Description: 10 mL in 1 PACKAGE

NDC 75936-164-04

Package Description: 5 mL in 1 PACKAGE

NDC 75936-164-05

Package Description: 1.5 mL in 1 PACKAGE

NDC 75936-164-06

Package Description: 15 mL in 1 TUBE

NDC 75936-164-07

Package Description: 30 mL in 1 TUBE

NDC 75936-164-08

Package Description: 20 mL in 1 CARTON

NDC Product Information

Unseen Sunscreen Broad Spectrum Spf 40 with NDC 75936-164 is a a human over the counter drug product labeled by Taylor James, Ltd.. The generic name of Unseen Sunscreen Broad Spectrum Spf 40 is avobenzone, homosalate, octinoxate, octisalate. The product's dosage form is cream and is administered via topical form.

Labeler Name: Taylor James, Ltd.

Dosage Form: Cream - An emulsion, semisolid3 dosage form, usually containing > 20% water and volatiles5 and/or < 50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.

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.

Unseen Sunscreen Broad Spectrum Spf 40 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.

  • AVOBENZONE 3 g/100mL
  • HOMOSALATE 8 g/100mL
  • OCTOCRYLENE 4 g/100mL
  • OCTISALATE 5 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.

  • ISODODECANE (UNII: A8289P68Y2)
  • DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6)
  • DIMETHICONE/BIS-ISOBUTYL PPG-20 CROSSPOLYMER (UNII: O4I3UFO6ZF)
  • ISOHEXADECANE (UNII: 918X1OUF1E)
  • DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
  • POLYESTER-7 (UNII: 0841698D2F)
  • NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)
  • POLYMETHYLSILSESQUIOXANE (11 MICRONS) (UNII: Z570VEV8XK)
  • MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
  • PHYMATOLITHON CALCAREUM (UNII: 6J1M3WA0ZK)
  • SHEA BUTTER (UNII: K49155WL9Y)
  • DIETHYLHEXYL SYRINGYLIDENEMALONATE (UNII: 3V5U97P248)
  • MANNITOL (UNII: 3OWL53L36A)
  • INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)
  • LECITHIN, SUNFLOWER (UNII: 834K0WOS5G)
  • MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
  • DIATOMACEOUS EARTH (UNII: 2RF6EJ0M85)
  • ZINC SULFATE (UNII: 89DS0H96TB)
  • SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
  • TOCOPHEROL (UNII: R0ZB2556P8)

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: Taylor James, Ltd.
Labeler Code: 75936
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: 10-10-2017 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: 12-31-2022 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 - NO 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.

Unseen Sunscreen Broad Spectrum Spf 40 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        PurposeAvobenzone 3%          SunscreenHomosalate 8%          SunscreenOctocrylene 4%         SunscreenOctisalate 5%             Sunscreen

Otc - Purpose

  • UsesHelps prevent sunburnIf used as directed with other sun protection measures (see Directions), decreases 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 or contact a Poison Control Center right away.

Indications & Usage

Stop use and ask a doctor if rash occurs

Warnings

WarningsFor external use onlyDo not use on damaged or broken skin

Dosage & Administration

  • Directionsapply generously and evenly 15 minutes before sun exposurereapply:after 40 minutes of swimming or sweatingimmediately after towel dryingat least every 2 hoursSun 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 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 sunglassesChildren under 6 months: ask a doctor

Inactive Ingredient

Inactive IngredientsIsododecane, Dimethicone Crosspolymer, Dimethicone/Bis-Isobutyl PPG-20 Crosspolymer, Polymethylsilsesquioxane, Isohexadecane, Dicrapylyl Carbonate, Meadowfoam Estolide, Caprylic/Capric Triglyceride, Polyester-7, Neopentyl Glycol Diheptanoate, Lithothamnion Calcareum Extract,Butyrospermum Parkii (Shea) Butter, Jojoba Esters, Mannitol, Boswellia Serrata Resin Extract, Lecithin, Microcrystalline Cellulose, Diatomaceous Earth, Zinc Sulfate, Silica, Tocopherol

* Please review the disclaimer below.