NDC 10967-660 Flesh Hydrating Spf Serum
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 10967 - Revlon Consumer Products Corporation
- 10967-660 - Flesh Hydrating Spf Serum
Product Packages
NDC Code 10967-660-01
Package Description: 30 mL in 1 PACKAGE
Product Details
What is NDC 10967-660?
What are the uses for Flesh Hydrating Spf Serum?
Which are Flesh Hydrating Spf Serum UNII Codes?
The UNII codes for the active ingredients in this product are:
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
Which are Flesh Hydrating Spf Serum 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:
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- GLYCERIN (UNII: PDC6A3C0OX)
- HONEY (UNII: Y9H1V576FH)
- AMMONIUM ACRYLOYLDIMETHYLTAURATE/BEHENETH-25 METHACRYLATE CROSSPOLYMER (52000 MPA.S) (UNII: LZ291VH90H)
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
- UREA (UNII: 8W8T17847W)
- HYDROXYCITRONELLAL (UNII: 8SQ0VA4YUR)
- LINALOOL, (+)- (UNII: F4VNO44C09)
- PUNICA GRANATUM ROOT BARK (UNII: CLV24I3T1D)
- SODIUM LACTATE (UNII: TU7HW0W0QT)
- ORNITHINE (UNII: E524N2IXA3)
- TROLAMINE (UNII: 9O3K93S3TK)
- .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- WATER (UNII: 059QF0KO0R)
- ARGININE HYDROCHLORIDE (UNII: F7LTH1E20Y)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- LYSINE HYDROCHLORIDE (UNII: JNJ23Q2COM)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- 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".