NDC 58400-006 Anti-aging Day Protect Spf 22
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 58400 - Pharmco Laboratories Inc.
- 58400-006 - Anti-aging Day Protect Spf 22
Product Packages
NDC Code 58400-006-01
Package Description: 87 g in 1 TUBE
NDC Code 58400-006-02
Package Description: 3900 g in 1 BOTTLE, PLASTIC
Product Details
What is NDC 58400-006?
What are the uses for Anti-aging Day Protect Spf 22?
Which are Anti-aging Day Protect Spf 22 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
Which are Anti-aging Day Protect Spf 22 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:
- ACETYL HEXAPEPTIDE-8 (UNII: L4EL31FWIL)
- ALOE (UNII: V5VD430YW9)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- TRICAPRIN (UNII: O1PB8EU98M)
- TRICAPRYLIN (UNII: 6P92858988)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- DIMETHICONE 350 (UNII: 2Y53S6ATLU)
- EDETATE SODIUM (UNII: MP1J8420LU)
- POLYISOBUTYLENE (1000 MW) (UNII: 5XB3A63Y52)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- OCTYLDODECANOL (UNII: 461N1O614Y)
- SQUALANE (UNII: GW89575KF9)
- PEG-100 STEARATE (UNII: YD01N1999R)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- 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".