NDC 41250-035 Meijer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 41250 - Meijer Distribution Inc
- 41250-035 - Meijer
Product Packages
NDC Code 41250-035-22
Package Description: 85 g in 1 BOTTLE
Product Details
What is NDC 41250-035?
What are the uses for Meijer?
Which are Meijer 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 Meijer 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)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- PEG-100 STEARATE (UNII: YD01N1999R)
- CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- XANTHAN GUM (UNII: TTV12P4NEE)
- TRIDECETH-6 (UNII: 3T5PCR2H0C)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- CHLORPHENESIN (UNII: I670DAL4SZ)
* 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".