NDC 71882-010 Everyday Uv Protector Sun Screen

NDC Product Code 71882-010

NDC CODE: 71882-010

Proprietary Name: Everyday Uv Protector Sun Screen 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.

NDC Code Structure

  • 71882 - Dermal Korea Co., Ltd

NDC 71882-010-01

Package Description: 15 g in 1 POUCH

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

NDC Product Information

Everyday Uv Protector Sun Screen with NDC 71882-010 is a product labeled by Dermal Korea Co., Ltd. The product's dosage form is and is administered via form.

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)
  • DIPROPYLENE GLYCOL (UNII: E107L85C40)

Product Labeler Information

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

Labeler Name: Dermal Korea Co., Ltd
Labeler Code: 71882
Start Marketing Date: 10-01-2017 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: 12-31-2019 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 - INACTIVATED, the listing data was inactivated by the FDA. 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.

Everyday Uv Protector Sun Screen Product Label Images

Everyday Uv Protector Sun Screen 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 Ingredient

Active ingredients: Homosalate 7.00%, Ethylhexyl Salicylate 4.50%, Butyl Methoxydibenzoylmethane 3.00%, Octocrylene 1.00%

Inactive Ingredient

Inactive ingredients: Water, Alcohol Denat., Dipropylene Glycol, Methyl Methacrylate Crosspolymer, Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine, Isoamyl p-Methoxycinnamate, Bis-PEG/PPG-20/5 PEG/PPG-20/5 Dimethicone, Methoxy PEG/PPG-25/4 Dimethicone, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Caprylic/Capric Triglyceride, Dimethicone, Caprylyl Glycol, Fragrance, Sodium Hydroxide, Ethylhexylglycerin, Centella Asiatica Extract, Adansonia Digitata Seed Extract, Aloe Barbadensis Leaf Extract, 1,2-Hexanediol, BHT, Disodium EDTA, Phenoxyethanol

Purpose

Purpose: Sunscreen

Warnings

Warnings: 1. Stop using if skin becomes red, swollen, itchy, etc during and after use. 2. Avoid using on irritated or sunburned skin by direct sunlight 3. Stop using on troubled skin part including eczema or dermatitis. 4. Avoid contact with the eyes. If contact occurs, rinse eyes thoroughly with water. 5. Keep away from the reach of baby and children. 6. Stored at room temperature only and keep away from direct sunlight.

Description

Uses: In the last step of skin care, apply evenly to the areas which are exposed to ultraviolet such as face, neck, arm, leg and so on.Directions: It protects your skin from UVA/UVB and keeps your skin soft all day long without being sticky!

* Please review the disclaimer below.