NDC 31645-204 The Healthy Powder Spf16
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 31645-204?
Which are The Healthy Powder Spf16 UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are The Healthy Powder Spf16 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:
- KAOLIN (UNII: 24H4NWX5CO)
- LAUROYL LYSINE (UNII: 113171Q70B)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- TOCOPHEROL (UNII: R0ZB2556P8)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- SQUALANE (UNII: GW89575KF9)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- TETRADIUM RUTICARPUM FRUIT (UNII: Q413WWJ3X9)
- STANNIC OXIDE (UNII: KM7N50LOS6)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- PROPANEDIOL (UNII: 5965N8W85T)
- WATER (UNII: 059QF0KO0R)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- MICA (UNII: V8A1AW0880)
- BORON NITRIDE (UNII: 2U4T60A6YD)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- O-CYMEN-5-OL (UNII: H41B6Q1I9L)
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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".