NDC 21839-011 Ultra Sensitive Faceblock Spf 25
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 21839-011?
Which are Ultra Sensitive Faceblock Spf 25 UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Ultra Sensitive Faceblock Spf 25 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)
- OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)
- ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- NEOPENTYL GLYCOL DIETHYLHEXANOATE (UNII: U68ZV6W62C)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PEG-100 STEARATE (UNII: YD01N1999R)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- NEOPENTYL GLYCOL DISOSTEARATE (UNII: 4M6OQ34JWW)
- MELISSA OFFICINALIS LEAF (UNII: 50D2ZE9219)
- CAMELLIA OLEIFERA LEAF (UNII: 5077EL0C60)
- ECHINACEA PURPUREA (UNII: QI7G114Y98)
- VITIS VINIFERA SEED (UNII: C34U15ICXA)
- LEMON PEEL (UNII: 72O054U628)
- CENTELLA ASIATICA (UNII: 7M867G6T1U)
- PROLINE (UNII: 9DLQ4CIU6V)
- MAGNESIUM ASCORBYL PHOSPHATE (UNII: 0R822556M5)
- PANTHENOL (UNII: WV9CM0O67Z)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- TOCOPHEROL (UNII: R0ZB2556P8)
- CITRUS MAXIMA FRUIT RIND OIL (UNII: 8U3877WD44)
- ROSEWOOD OIL (UNII: F2522O5L7B)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- THYME OIL (UNII: 2UK410MY6B)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- XANTHAN GUM (UNII: TTV12P4NEE)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- SODIUM LACTATE (UNII: TU7HW0W0QT)
- SORBITOL (UNII: 506T60A25R)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- TALC (UNII: 7SEV7J4R1U)
- GERANIOL (UNII: L837108USY)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
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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".