NDC 42952-101 I-max Excellence
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 42952 - Maxlife Usa, Inc.
- 42952-101 - I-max Excellence
Product Packages
NDC Code 42952-101-12
Package Description: 59 mL in 1 BOTTLE
Product Details
What is NDC 42952-101?
What are the uses for I-max Excellence?
Which are I-max Excellence UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are I-max Excellence 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:
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- CARBOMER INTERPOLYMER TYPE A (55000 MPA.S) (UNII: 59TL3WG5CO)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- CETYL PHOSPHATE (UNII: VT07D6X67O)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- STEARETH-20 (UNII: L0Q8IK9E08)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- 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".