NDC 59663-001 Moisturizing Sunscreen Spf15
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 59663 - Shine & Pretty (usa), Corp.
- 59663-001 - Moisturizing Sunscreen Spf15
Product Packages
NDC Code 59663-001-01
Package Description: 100 mL in 1 BOTTLE
Product Details
What is NDC 59663-001?
What are the uses for Moisturizing Sunscreen Spf15?
Which are Moisturizing Sunscreen Spf15 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Moisturizing Sunscreen Spf15 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:
- SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- CARBOMER 934 (UNII: Z135WT9208)
- VITAMIN E ACETATE (UNII: 9E8X80D2L0)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- TROLAMINE (UNII: 9O3K93S3TK)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- WATER (UNII: 059QF0KO0R)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- CHAMAEMELUM NOBILE FLOWER (UNII: O2T154T6OG)
* 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".