NDC 70618-006 Sun Project Water Sun Cream Spf50
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 70618-006?
What are the uses for Sun Project Water Sun Cream Spf50?
Which are Sun Project Water Sun Cream Spf50 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Sun Project Water Sun Cream Spf50 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)
- DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE (UNII: ANQ870JD20)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CYCLOMETHICONE (UNII: NMQ347994Z)
- ALCOHOL (UNII: 3K9958V90M)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- DOCOSANOL (UNII: 9G1OE216XY)
- PEG-100 STEARATE (UNII: YD01N1999R)
- VISCUM ALBUM FRUITING TOP (UNII: BK9092J5MP)
- CENTELLA ASIATICA (UNII: 7M867G6T1U)
- PURSLANE (UNII: M6S840WXG5)
- SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX)
- ISOHEXADECANE (UNII: 918X1OUF1E)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ALUMINUM STEARATE (UNII: U6XF9NP8HM)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- OCTYLDODECANOL (UNII: 461N1O614Y)
- BAMBUSA VULGARIS WHOLE (UNII: WCD45M1BSK)
- XANTHAN GUM (UNII: TTV12P4NEE)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- ECHIUM PLANTAGINEUM SEED OIL (UNII: PIB7XBU8XW)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ALCEA ROSEA FLOWER (UNII: 1250O8MKPZ)
- CARDIOSPERMUM HALICACABUM FLOWERING TOP (UNII: MZP2508BRR)
- PLUKENETIA VOLUBILIS SEED OIL (UNII: 8ED72Z8J1Z)
* Please review the disclaimer below.
[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".