NDC 72019-0001 Riversol Lightweight Broad Spectrum Sunscreen Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72019 - Riversol Skincare Solutions Inc
- 72019-0001 - Riversol Lightweight Broad Spectrum Sunscreen Spf 30
Product Characteristics
Product Packages
NDC Code 72019-0001-1
Package Description: 1 BOTTLE in 1 BOX / 60 mL in 1 BOTTLE
Product Details
What is NDC 72019-0001?
What are the uses for Riversol Lightweight Broad Spectrum Sunscreen Spf 30?
Which are Riversol Lightweight Broad Spectrum Sunscreen Spf 30 UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Riversol Lightweight Broad Spectrum Sunscreen Spf 30 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)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- VITIS VINIFERA SEED (UNII: C34U15ICXA)
- GLYCERIN (UNII: PDC6A3C0OX)
- ORYZA SATIVA WHOLE (UNII: 84IVV0906Z)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- MAURITIA FLEXUOSA FRUIT OIL (UNII: 48H19MS04L)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- XANTHAN GUM (UNII: TTV12P4NEE)
- LAURIC ACID (UNII: 1160N9NU9U)
- STARCH, TAPIOCA (UNII: 24SC3U704I)
- ALCOHOL (UNII: 3K9958V90M)
- AMINOPROPYL ASCORBYL PHOSPHATE (UNII: 290O2PQ83R)
- DISODIUM LAURIMINODIPROPIONATE TOCOPHERYL PHOSPHATE (UNII: 408UEF2TE8)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- SORBIC ACID (UNII: X045WJ989B)
- CAPRYLIC/CAPRIC ACID (UNII: DI775RT244)
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- CITRIC ACID ACETATE (UNII: DSO12WL7AU)
- SIMMONDSIA CHINENSIS SEED (UNII: D24K2Q1F6H)
- GLYCERYL ISOSTEARATE (UNII: HYE7O27HAO)
- POLYHYDROXYSTEARIC ACID STEARATE (UNII: 8KQ7I65XZE)
- HIPPOPHAE RHAMNOIDES SEED OIL (UNII: T53SBG6741)
- MICA (UNII: V8A1AW0880)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- .BETA.-THUJAPLICIN (UNII: U5335D6EBI)
- CETEARYL OLIVATE (UNII: 58B69Q84JO)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
* 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".