NDC 55789-2902 Mineral Spf 30 Sun
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
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Product Details
What is NDC 55789-2902?
What are the uses for Mineral Spf 30 Sun?
Which are Mineral Spf 30 Sun 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 Mineral Spf 30 Sun 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:
- COCONUT OIL (UNII: Q9L0O73W7L)
- COCOA BUTTER (UNII: 512OYT1CRR)
- CASTOR OIL (UNII: D5340Y2I9G)
- LINSEED OIL (UNII: 84XB4DV00W)
- ROSA CANINA FLOWER OIL (UNII: DUY7M48I1T)
- GINKGO (UNII: 19FUJ2C58T)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- ROSEMARY (UNII: IJ67X351P9)
- SHEANUT OIL (UNII: O88E196QRF)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- WATER (UNII: 059QF0KO0R)
- BORAGE OIL (UNII: F8XAG1755S)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
- CITRUS SINENSIS FLOWER WAX (UNII: 8L3Z7JK2NU)
- THYMOPENTIN (UNII: O3Y80ZF13F)
- TEA LEAF OIL (UNII: VC855RRT77)
- CHAMOMILE FLOWER OIL (UNII: 60F80Z61A9)
- CUCUMIS SATIVUS LEAF (UNII: Q6S42514LP)
- CEDRUS ATLANTICA BARK OIL (UNII: ZX5QRE4U60)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- PELARGONIUM GRAVEOLENS FLOWER OIL (UNII: 3K0J1S7QGC)
- VANILLA PLANIFOLIA OIL (UNII: 0A3F415158)
- PANTHENOL (UNII: WV9CM0O67Z)
- ALLANTOIN (UNII: 344S277G0Z)
- TOCOPHEROL (UNII: R0ZB2556P8)
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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".