NDC 11822-7788 Tanning Sunscreen Spf 4 Daylogic
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 11822 - Rite Aid
- 11822-7788 - Tanning Sunscreen Spf 4
Product Packages
NDC Code 11822-7788-6
Package Description: 236 mL in 1 BOTTLE
Product Details
What is NDC 11822-7788?
Which are Tanning Sunscreen Spf 4 Daylogic UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Tanning Sunscreen Spf 4 Daylogic 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 (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- AMMONIA (UNII: 5138Q19F1X)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- MINERAL OIL (UNII: T5L8T28FGP)
- PEG-40 CASTOR OIL (UNII: 4ERD2076EF)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- SORBITOL (UNII: 506T60A25R)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- COCOA BUTTER (UNII: 512OYT1CRR)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- TROLAMINE (UNII: 9O3K93S3TK)
- WATER (UNII: 059QF0KO0R)
* 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".