NDC 72019-0004 Riversol Spf 40 Weightless Body Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 72019-0004?
What are the uses for Riversol Spf 40 Weightless Body Sunscreen?
Which are Riversol Spf 40 Weightless Body Sunscreen UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Riversol Spf 40 Weightless Body 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:
- AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)
- METHYLCELLULOSE (100 CPS) (UNII: 4GFU244C4J)
- XANTHAN GUM (UNII: TTV12P4NEE)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- PHYTATE SODIUM (UNII: 88496G1ERL)
- LONICERA CAPRIFOLIUM FLOWER (UNII: 5N1WD9784U)
- GINKGO BILOBA WHOLE (UNII: 660486U6OI)
- CAMELLIA SINENSIS WHOLE (UNII: C5M4585ZBZ)
- BAMBUSA ARUNDINACEA STEM (UNII: NRA4497HC5)
- POLYGLYCERYL-4 OLEATE (UNII: 15B05TY4GX)
- GLUCONOLACTONE (UNII: WQ29KQ9POT)
- HYDROGENATED METHYL ABIETATE (UNII: A23O709X8O)
- SORBITAN MONOLAURATE (UNII: 6W9PS8B71J)
- JOJOBA OIL (UNII: 724GKU717M)
- LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
- LONICERA JAPONICA FLOWER (UNII: 4465L2WS4Y)
- POPULUS TREMULOIDES BARK (UNII: 5543O0CEID)
- TOCOPHEROL (UNII: R0ZB2556P8)
- OCTYLDODECYL LACTATE (UNII: 8JKW8M5W35)
- SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- SODIUM LAURYL GLYCOL CARBOXYLATE (UNII: 8L0472VMYL)
- SOYBEAN OIL (UNII: 241ATL177A)
- WATER (UNII: 059QF0KO0R)
- ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE (UNII: D2QHA03458)
- GLYCERIN (UNII: PDC6A3C0OX)
- DILAURYL CITRATE (UNII: 5OYS3G306B)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
* 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".