NDC 51060-196 Rainforest Of The Sea Water Foundation Broad Spectrum Spf 15 Sunscreen 61h Mahogany
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 51060-196?
What are the uses for Rainforest Of The Sea Water Foundation Broad Spectrum Spf 15 Sunscreen 61h Mahogany?
Which are Rainforest Of The Sea Water Foundation Broad Spectrum Spf 15 Sunscreen 61h Mahogany 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 Rainforest Of The Sea Water Foundation Broad Spectrum Spf 15 Sunscreen 61h Mahogany 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- ISODODECANE (UNII: A8289P68Y2)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- NYLON-12 (UNII: 446U8J075B)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
- MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)
- PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE (UNII: TYP81E471F)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)
- STEARALKONIUM HECTORITE (UNII: OLX698AH5P)
- POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
- HEXYL LAURATE (UNII: 4CG9F9W01Q)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- PROPYLENE CARBONATE (UNII: 8D08K3S51E)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- COCONUT OIL (UNII: Q9L0O73W7L)
- GARDENIA TAITENSIS FLOWER (UNII: T0OCU8201Y)
- TOCOPHEROL (UNII: R0ZB2556P8)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- LAURYL PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE (UNII: 25G622K2RA)
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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".