NDC 64048-1235 Ultimate Sheer Sunscreen Spf 70 Daylogic
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 64048 - Product Quiest Mfg
- 64048-1235 - Ultimate Sheer Sunscreen Spf 70
Product Packages
NDC Code 64048-1235-2
Package Description: 43 g in 1 PACKAGE
Product Details
What is NDC 64048-1235?
Which are Ultimate Sheer Sunscreen Spf 70 Daylogic 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 Ultimate Sheer Sunscreen Spf 70 Daylogic 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:
- YELLOW WAX (UNII: 2ZA36H0S2V)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- NEOPENTYL GLYCOL DIETHYLHEXANOATE (UNII: U68ZV6W62C)
- NEOPENTYL GLYCOL DIISOSTEARATE (UNII: 4M6OQ34JWW)
- OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)
- CERESIN (UNII: Q1LS2UJO3A)
- PARAFFIN (UNII: I9O0E3H2ZE)
- PETROLATUM (UNII: 4T6H12BN9U)
- POLYESTER-8 (1400 MW, CYANODIPHENYLPROPENOYL CAPPED) (UNII: T9296U138P)
- HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
* 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".