NDC 50390-707 Peter Island Ultimate Sheer Dry Touch Sunscreen Spf 70

Homosalate, Oxybenzone, Octisalate, Avobenzone, Octocrylene

NDC Product Code 50390-707

NDC Code: 50390-707

Proprietary Name: Peter Island Ultimate Sheer Dry Touch Sunscreen Spf 70 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: Homosalate, Oxybenzone, Octisalate, Avobenzone, Octocrylene 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

  • 50390 - Amway Corp.
    • 50390-707 - Peter Island Ultimate Sheer Dry Touch Sunscreen

NDC 50390-707-12

Package Description: 85 g in 1 BOTTLE, PLASTIC

NDC Product Information

Peter Island Ultimate Sheer Dry Touch Sunscreen Spf 70 with NDC 50390-707 is a a human over the counter drug product labeled by Amway Corp.. The generic name of Peter Island Ultimate Sheer Dry Touch Sunscreen Spf 70 is homosalate, oxybenzone, octisalate, avobenzone, octocrylene. The product's dosage form is lotion and is administered via topical form.

Labeler Name: Amway Corp.

Dosage Form: Lotion - An emulsion, liquid1 dosage form. This dosage form is generally for external application to the skin.2

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.

Peter Island Ultimate Sheer Dry Touch Sunscreen Spf 70 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.

  • HOMOSALATE 15 g/100g
  • OXYBENZONE 6 g/100g
  • AVOBENZONE 3 g/100g
  • OCTISALATE 5 g/100g
  • OCTOCRYLENE 2.8 g/100g

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)
  • PEG-100 STEARATE (UNII: YD01N1999R)

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: Amway Corp.
Labeler Code: 50390
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: 11-26-2012 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2018 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: E 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.

Peter Island Ultimate Sheer Dry Touch Sunscreen Spf 70 Product Label Images

Peter Island Ultimate Sheer Dry Touch Sunscreen Spf 70 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

Active Ingredients

Homosalate 15.0%Oxybenzone 6.0%Octisalate 5.0%Avobenzone 3.0%Octocrylene 2.8%


FOR EXTERNAL USE ONLY.Avoid contact with eyes. Rinse with water if contact occurs.

Otc - Stop Use

Discontinue use if signs of rash or irritation develop.

Otc - Ask Doctor

For use on children under the age of 6 months consult a physician.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.


Apply generously and evenly 30 minutes before sun exposure. Reapply frequently and after swimming, excessive perspiration and towel drying.

Other Information

  • May stain some fabricsSun Alert: Limiting sun exposure, wearing protective clothing, and using sunscreens may reduce the risks of skin aging, skin cancer, and other harmful effects of the sun.


This Sheer Dry-Touch Sunscreen provides Broad Spectrum UVA/UVB protection from the sun's damaging rays. It's PABA free,oil-free and non-greasy. This light weight formula is dermatologist tested, offers a light fresh scent and is very water resistant.

Inactive Ingredients

Water, Styrene/Acrylates Copolymer, Butyloctyl Salicylate, Glyceryl Stearate, Silica, PEG-100 Stearate, Acrylates/C12-22 Alkyl Methacrylate Copolymer, Caprylyl Methicone, Sodium Polyacrylate, Benzyl Alcohol, Beeswax, Ethylhexyl Stearate, Dimethicone, Cetyl Dimethicone, Xanthan Gum, Trimethylsiloxysilicate, Trideceth-6, Disodium EDTA, Dipotassium Glycyrrhizate, BHT, Chlorphenesin

* Please review the disclaimer below.

Previous Code
Next Code