NDC 82328-0012 Sheer Daily Wear Face Protection Mineral Based Sunscreen Spf 16
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 82328-0012?
What are the uses for Sheer Daily Wear Face Protection Mineral Based Sunscreen Spf 16?
Which are Sheer Daily Wear Face Protection Mineral Based Sunscreen Spf 16 UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
Which are Sheer Daily Wear Face Protection Mineral Based Sunscreen Spf 16 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)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP)
- COCONUT OIL (UNII: Q9L0O73W7L)
- SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
- POLYGLYCERYL-10 LAURATE (UNII: MPJ2Q8WI8G)
- GLYCERIN (UNII: PDC6A3C0OX)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)
- GLUCONOLACTONE (UNII: WQ29KQ9POT)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SANDALWOOD OIL (UNII: X7X01WMQ5F)
- XANTHAN GUM (UNII: TTV12P4NEE)
- JOJOBA OIL (UNII: 724GKU717M)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- CALCIUM GLUCONATE (UNII: SQE6VB453K)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R)
- PALMITOYL HEXAPEPTIDE-12 (UNII: HO4ZT5S86C)
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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".