NDC 42877-001 Skin Effects Firming Facial With Retinol Complex Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 42877 - Diversified Global Technologies Dba Diversified Distribution
- 42877-001 - Skin Effects Firming Facial With Retinol Complex Spf 30
Product Packages
NDC Code 42877-001-01
Package Description: 28.3 g in 1 BOTTLE
Product Details
What is NDC 42877-001?
What are the uses for Skin Effects Firming Facial With Retinol Complex Spf 30?
Which are Skin Effects Firming Facial With Retinol Complex Spf 30 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)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
Which are Skin Effects Firming Facial With Retinol Complex Spf 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)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- SHEA BUTTER (UNII: K49155WL9Y)
- ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
- CETETH-20 (UNII: I835H2IHHX)
- STEARETH-2 (UNII: V56DFE46J5)
- SQUALANE (UNII: GW89575KF9)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PEG-75 STEARATE (UNII: OT38R0N74H)
- .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
- RETINOL (UNII: G2SH0XKK91)
- TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
- ALLANTOIN (UNII: 344S277G0Z)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- LAURETH-7 (UNII: Z95S6G8201)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- O-CYMEN-5-OL (UNII: H41B6Q1I9L)
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[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".