NDC 70218-030 Srb 3 Lighting White Sun

NDC Product Code 70218-030

NDC CODE: 70218-030

Proprietary Name: Srb 3 Lighting White Sun 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

  • 70218 - Casinbio Co., Ltd.

NDC 70218-030-01

Package Description: 50 mL in 1 CARTON

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

NDC Product Information

Srb 3 Lighting White Sun with NDC 70218-030 is a product labeled by Casinbio 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)
  • BUTYLENE GLYCOL (UNII: 3XUS85K0RA)

Product Labeler Information

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

Labeler Name: Casinbio Co., Ltd.
Labeler Code: 70218
Start Marketing Date: 10-01-2015 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 - 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.

Srb 3 Lighting White Sun Product Label Images

Srb 3 Lighting White Sun 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 Ingredient: Ethylhexyl Methoxycinnamate 7.50%, Ethylhexyl Salicylate 5.00%, Butyl Methoxydibenzoylmethane 3.00%

Inactive Ingredient

Inactive Ingredients: Water, Butylene Glycol, Caprylic/Capric Triglyceride, Phenylbenzimidazole Sulfonic Acid, Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine, Niacinamide, Cetearyl Alcohol, Methyl Methacrylate Crosspolymer, Cyclopentasiloxane, Glyceryl Stearate, Cetearyl Olivate, Glycerin, Sorbitan Olivate, Oryza Sativa (Rice) Bran Extract, Sodium Hydroxide, Cyclohexasiloxane, Nylon-12, Polyacrylate-13, Sorbitan Stearate, Dimethicone, PEG-100 Stearate, Caprylyl Glycol, Polyisobutene, Ethylhexylglycerin, Tocopheryl Acetate, Fragrance, Disodium EDTA, Dextrin, 1,2-Hexanediol, Polysorbate 20, Sorbitan Isostearate, BHT, Citrus Aurantifolia (Lime) Flower Extract, Prunus Persica (Peach) Flower Extract, Propylene Glycol, Pyrus Malus (Apple) Flower Extract, Ananas sativus (pineapple) fruit Extract, Actinidia Chinensis (Kiwi) Fruit Extract, Alchemilla Vulgaris Extract, Arnica Montana Flower Extract, Vaccinium Macrocarpon (Cranberry) Fruit Extract, Adansonia Digitata Seed Extract, Equisetum Arvense Extract, Olea Europaea (Olive) Leaf Extract, Punica Granatum Flower Extract, Prunus Avium (Sweet Cherry) Flower Extract, Citrus Aurantium Dulcis (Orange) Flower Extract, Sophora Japonica Flower Extract, Fructan, Phenoxyethanol

Purpose

Purpose: Sunscreen

Warnings

Warnings: 1. If the following side effects occur, immediately discontinue use. Before resuming use, consult a dermatologist as continual use may worsen symptoms. A) If red spots, swelling, itching, irritation, or other discomforts occur after using the product. B) If the above symptoms occur on the applied area after exposure to direct sunlight. 2. Do not use on open wounds or on areas of skin exhibiting signs of eczema or dermatitis. 3. Storage and handling precautions A) Keep product out of reach of infants and children. B) Ensure that lid is closed after use. C) Do not store in places subject to high or cold temperatures or under exposure to direct sunlight. D) Use care to avoid eye contact when using this product.

Description

How to use: Apply an appropriate amount to areas exposed to sunlight such as the face, neck, arms, legs, and spread evenly.Recommended dosage: Spread an appropriate amount over areas exposed to sunlight such as the face, neck, arms, and legs

* Please review the disclaimer below.