NDC 44717-538 Natria Brightening Spf 15

NDC Product Code 44717-538

NDC 44717-538-02

Package Description: 1 BOTTLE in 1 BOX > 50 mL in 1 BOTTLE (44717-538-01)

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

NDC Product Information

Natria Brightening Spf 15 with NDC 44717-538 is a product labeled by Wasatch Product Development. The generic name of Natria Brightening Spf 15 is . The product's dosage form is and is administered via form.

Labeler Name: Wasatch Product Development

Dosage Form: -

Product Type: 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.

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.


Product Labeler Information

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

Labeler Name: Wasatch Product Development
Labeler Code: 44717
Start Marketing Date: 07-19-2010 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: 12-31-2017 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 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.

Natria Brightening Spf 15 Product Label Images

Natria Brightening 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 IngredientsEthylhexyl Methoxycinnamate 7.5%Zinc Oxide 4%

Otc - Purpose

Provides instant hydration and long- lasting defense against UV rays to keep skin clear from discoloration

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.

Indications & Usage

For external use only.


Avoid contact with eyes. Rinse with water if eye contact occurs. Discontinue use and contact a doctor if rash or irritation develops and persists.

Dosage & Administration

With fingertips, smooth gently and evenly over face and neck .

Inactive Ingredient

Ingredients: Water (Aqua), Cyclopentasiloxane, Cetearyl Glucoside, Isopentyldiol, C12-15 Alkyl Benzoate, Dimethicone, Glycyrrhiza Glabra (Licorice) Root Extract, Morus Alba (Mulberry) Root Extract, Plankton Extract, Farnesyl Acetate, Farnesol, Glycine Soja (Soybean) Lipids, Retinyl Palmitate (Vitamin A), Panthenyl Triacetate (Vitamin B), Tetrahexyldecyl Ascorbate (Vitamin C), Tocopheryl Acetate (Vitamin E), Aloe Barbadensis, Camellia Oleifera (Green Tea) Leaf Extract, Chamomilla Recutita (Matricaria) Flower Extract, Ginkgo Biloba Leaf Extract, Panax Ginseng Root Extract, Ulva Lactuca (Sea Lettuce) Extract, Vitis Vinifera (Grape) Seed Extract, Fragrance (Essential Oils), Squalane, Zea Mays (Corn) Oil, Algae Extract, Artemisia Princeps Leaf Extract, Sodium PCA, Ergothioneine, Caprylic/Capric Triglyceride, Behenyl Alcohol, Magnesium Aluminu Silicate, Butylene Glycol, Lecithin, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Polysorbate 60, Xanthan Gum, Disodium EDTA, Sodium Hydroxide, Glycerin, Phenoxyethanol, Chlorphenesin, Methylparaben, Benzoic Acid.

* Please review the disclaimer below.