NDC 41250-012 Meijer Oil Free 30
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 41250 - Meijer Distribution Inc
- 41250-012 - Meijer Oil Free 30
Product Packages
NDC Code 41250-012-56
Package Description: 236 mL in 1 BOTTLE
Product Details
What is NDC 41250-012?
What are the uses for Meijer Oil Free 30?
Which are Meijer Oil Free 30 UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Meijer Oil Free 30 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)
- 2-ETHYLHEXYL BENZOATE (UNII: R63ZWW1A13)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
- DIISOPROPYL ADIPATE (UNII: P7E6YFV72X)
- NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)
- PHENETHYL BENZOATE (UNII: 0C143929GK)
- POLYMETHYLSILSESQUIOXANE (11 MICRONS) (UNII: Z570VEV8XK)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- GLYCERIN (UNII: PDC6A3C0OX)
- TROLAMINE (UNII: 9O3K93S3TK)
- COCO GLUCOSIDE (UNII: ICS790225B)
- CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)
- CETETH-10 PHOSPHATE (UNII: 4E05O5N49G)
- DIHEXADECYL PHOSPHATE (UNII: 2V6E5WN99N)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- PARAFFIN (UNII: I9O0E3H2ZE)
- TOCOPHEROL (UNII: R0ZB2556P8)
- SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
* 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".