NDC 76214-032 Cactus Whitening Sun Spf 34 Pa Plus Plus For Men
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 76214 - Skinfood Co., Ltd.
- 76214-032 - Cactus Whitening Sun
Product Packages
NDC Code 76214-032-01
Package Description: 70 mL in 1 BOTTLE
Product Details
What is NDC 76214-032?
What are the uses for Cactus Whitening Sun Spf 34 Pa Plus Plus For Men?
Which are Cactus Whitening Sun Spf 34 Pa Plus Plus For Men 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)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM (UNII: D1JT611TNE) (Active Moiety)
Which are Cactus Whitening Sun Spf 34 Pa Plus Plus For Men 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)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- ARBUTIN (UNII: C5INA23HXF)
- C14-22 ALCOHOLS (UNII: B1K89384RJ)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
- C12-20 ALKYL GLUCOSIDE (UNII: K67N5Z1RUA)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CUCUMBER (UNII: YY7C30VXJT)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ISOHEXADECANE (UNII: 918X1OUF1E)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
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[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".