NDC 21839-111 Faceblock Spf30 Super Sensitive
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
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Product Details
What is NDC 21839-111?
Which are Faceblock Spf30 Super Sensitive UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Faceblock Spf30 Super Sensitive 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)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- DICAPRYLYL ETHER (UNII: 77JZM5516Z)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- LAVANDIN OIL (UNII: 9RES347CKG)
- ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- LINALOOL, DL- (UNII: D81QY6I88E)
- EDETATE SODIUM (UNII: MP1J8420LU)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
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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".