NDC 69352-020 Amarte Ultra Veil Ultra Light Sunscreen Fluid

Product Information

Product Code69352-020
Proprietary Name 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.
Amarte Ultra Veil Ultra Light Sunscreen Fluid
Product Labeler Information What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.
Amarteinternational Co., Ltd.
Labeler Code69352
Start Marketing Date 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 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 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".
NDC Code Structure

Usage Information

Product Packages

NDC 69352-020-01

Package Description: 70 mL in 1 CARTON

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

Product Details

Amarte Ultra Veil Ultra Light Sunscreen Fluid is product labeled by Amarteinternational Co., Ltd.. The product's dosage form is and is administered via form.

What are Amarte Ultra Veil Ultra Light Sunscreen Fluid Active Ingredients?

The following is the list of active ingredients in this product. An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

  • OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
  • TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
  • OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
  • ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)

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)

* Please review the disclaimer below.

Amarte Ultra Veil Ultra Light Sunscreen Fluid Labeling and Warnings

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Table of Contents

Active Ingredient

Active Ingredients: Ethylhexyl Methoxycinnamate 7.0%, Titanium Dioxide 5.4%, Ethylhexyl Salicylate 5.0%, Zinc Oxide 3.0%

Inactive Ingredient

Inactive Ingredients:
cyclomethicone, water, cyclopentasiloxane, glycerin, butylene glycol, alcohol, silica, mica, cyclohexasiloxane, PEG-10 dimethicone, cetyl PEG/PPG-10/1 dimethicone, sorbitan sesquioleate, hexyl laurate, dimethicone, caviar extract, Ginkgo biloba nut extract, Phellinus linteus extract, sodium hyaluronate, elemental sulfur, Aspalathus linearis extract, Potentilla erecta root extract, Scutellaria, baicalensis root extract, human oligopeptide-1, Thymus serpyllum extract, stearic acid, alumina, isostearic acid, triethoxycaprylylsilane, stearalkonium hectorite, disodium EDTA, fragrance, phenoxyethanol, BHT




For external use only
Do not use on damaged or broken skin.
When using this product keep out of eyes. Rinse with water to remove.
Stop use and ask a doctor if rash occurs.
Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

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.


- helps prevent sunburn
- if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun


- apply liberally 15 minutes before sun exposure
- reapply:
- after 40 minutes of swimming or sweating
- immediately after towel drying
- at least every 2 hours
- children under 6 months: Ask a doctor
- 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

* Please review the disclaimer below.