NDC 11822-1840 Rite Aid Sport Spf 50
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 11822 - Rite Aid
- 11822-1840 - Rite Aid Sport Spf 50
Product Packages
NDC Code 11822-1840-6
Package Description: 236 g in 1 BOTTLE
Product Details
What is NDC 11822-1840?
What are the uses for Rite Aid Sport Spf 50?
Which are Rite Aid Sport Spf 50 UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Rite Aid Sport Spf 50 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)
- NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PEG-100 STEARATE (UNII: YD01N1999R)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- TOCOPHEROL (UNII: R0ZB2556P8)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)
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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".