NDC 70784-006 Pollen Uv Perfect Daily Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70784 - Nsb Co., Ltd.
- 70784-006 - Pollen Uv Perfect Daily Sunscreen
Product Packages
NDC Code 70784-006-02
Package Description: 1 CONTAINER in 1 PACKAGE / 50 mL in 1 CONTAINER (70784-006-01)
Product Details
What is NDC 70784-006?
What are the uses for Pollen Uv Perfect Daily Sunscreen?
Which are Pollen Uv Perfect Daily Sunscreen UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Pollen Uv Perfect Daily Sunscreen Inactive Ingredients UNII Codes?
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. The UNII codes for the inactive ingredients in this product are:
- WATER (UNII: 059QF0KO0R)
- PANTHENOL (UNII: WV9CM0O67Z)
- NIACINAMIDE (UNII: 25X51I8RD4)
- ENSULIZOLE (UNII: 9YQ9DI1W42)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- TROMETHAMINE (UNII: 023C2WHX2V)
- C14-22 ALCOHOLS (UNII: B1K89384RJ)
- BISOCTRIZOLE (UNII: 8NT850T0YS)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- BEMOTRIZINOL (UNII: PWZ1720CBH)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PEG-100 STEARATE (UNII: YD01N1999R)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- SHEA BUTTER (UNII: K49155WL9Y)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- C12-20 ALKYL GLUCOSIDE (UNII: K67N5Z1RUA)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- XANTHAN GUM (UNII: TTV12P4NEE)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
- HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
- BEE POLLEN (UNII: 3729L8MA2C)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] 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.
[12] 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".