NDC 59078-326 Tako Pore Sebum Sun
NDC Product Code 59078-326
Proprietary Name: Tako Pore Sebum 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
- 59078 - Tony Moly Co.,ltd
- 59078-326 - Tako Pore Sebum Sun
NDC 59078-326-02
Package Description: 1 CONTAINER in 1 CARTON > 9.5 g in 1 CONTAINER (59078-326-01)
NDC Product Information
Tako Pore Sebum Sun with NDC 59078-326 is a product labeled by Tony Moly 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.
- DIMETHICONE (UNII: 92RU3N3Y1O)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
Product Labeler Information
What is the Labeler Name?Name of Company corresponding to the labeler code segment of the Product NDC.
Labeler Name: Tony Moly Co.,ltd
Labeler Code: 59078
Start Marketing Date: 03-01-2018 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".
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Tako Pore Sebum Sun Product Label Images
Tako Pore Sebum 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 ingredients: Octocrylene 5.00%, Homosalate 5.00%, Ethylhexyl Salicylate 4.50%, Butyl Methoxydibenzoylmethane 4.00%, Ethylhexyl Methoxycinnamate 3.50%
Inactive Ingredient
Inactive ingredients:Dimethicone, Polyethylene, Ethylhexyl Palmitate, Vinyl Dimethicone/Methicone Silsesquioxane Crosspolymer, Diphenylsiloxy Phenyl Trimethicone, Microcrystalline Wax, Polysilicone-15, Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine, Fragrance, Tocopheryl Acetate, Caprylyl Glycol, Eclipta Prostrata Extract, Melia Azadirachta Leaf Extract, Moringa Oleifera Seed Oil, Water, Panthenol, Calamine, Nelumbo Nucifera Flower Water, Sea Water, Centella Asiatica Extract, 1,2-Hexanediol, Algae Extract, Chlorella Vulgaris Extract, Hizikia Fusiforme Extract, Hydrolyzed Collagen
Purpose
Purpose: Sunscreen
Warnings
Warnings:For external use onlyAvoid contact with eyes.Discontinue use if signs of irritation or rashes appear.Replace the cap after use.Keep Out of Reach of Children
Description
Uses:- helps prevent sunburn- If used as directed with other sun protection measuresDirections:Take an appropriate amount, evenly apply to face and body anywhere to be exposed to UV rays. Use as the last step of basic skin care.
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