NDC 70281-504 Ocean Potion Spf30 Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70281 - Solskyn Personal Care Llc
- 70281-504 - Ocean Potion Spf30 Sunscreen
Product Packages
NDC Code 70281-504-24
Package Description: 100 mg in 1 BOTTLE
Product Details
What is NDC 70281-504?
What are the uses for Ocean Potion Spf30 Sunscreen?
Which are Ocean Potion Spf30 Sunscreen UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (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)
Which are Ocean Potion Spf30 Sunscreen 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:
- CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- DIISOPROPYL ADIPATE (UNII: P7E6YFV72X)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- HYDROGENATED PALM GLYCERIDES (UNII: YCZ8EM144Q)
- LAMINARIA SACCHARINA EXTRACT (UNII: 68CMP2MB55)
- MACROCYSTIS PYRIFERA (UNII: K31S3OG5C4)
- NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)
- PEG-16 MACADAMIA GLYCERIDES (UNII: 2OTC93KMHU)
- PEG-100 STEARATE (UNII: YD01N1999R)
- PHENETHYL BENZOATE (UNII: 0C143929GK)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- THERMUS THERMOPHILUS LYSATE (UNII: 775R692494)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- TRISILOXANE (UNII: 9G1ZW13R0G)
- WATER (UNII: 059QF0KO0R)
- XANTHAN GUM (UNII: TTV12P4NEE)
* 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".