NDC 11822-9014 Rite Aid Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 11822 - Rite Aid Corporation
- 11822-9014 - Rite Aid Sunscreen
Product Packages
NDC Code 11822-9014-9
Package Description: 453 g in 1 BOTTLE, PLASTIC
Product Details
What is NDC 11822-9014?
What are the uses for Rite Aid Sunscreen?
Which are Rite Aid Sunscreen UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Rite Aid 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:
- WATER (UNII: 059QF0KO0R)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- MINERAL OIL (UNII: T5L8T28FGP)
- TROLAMINE (UNII: 9O3K93S3TK)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- GLYCOL STEARATE (UNII: 0324G66D0E)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
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[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".