NDC 57913-2857 Oil-control Day Spf 15
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 57913 - Erno Laszlo, Inc.
- 57913-2857 - Oil-control Day Spf 15
Product Packages
NDC Code 57913-2857-8
Package Description: 1 BOTTLE in 1 CARTON / 90 mL in 1 BOTTLE
Product Details
What is NDC 57913-2857?
What are the uses for Oil-control Day Spf 15?
Which are Oil-control Day Spf 15 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)
Which are Oil-control Day Spf 15 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)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- GLYCERIN (UNII: PDC6A3C0OX)
- PEG-100 STEARATE (UNII: YD01N1999R)
- SACCHARIDE ISOMERATE (UNII: W8K377W98I)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- OCTYLDODECANOL (UNII: 461N1O614Y)
- CETETH-20 (UNII: I835H2IHHX)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- SQUALANE (UNII: GW89575KF9)
- ARACHIDYL PROPIONATE (UNII: QV5DAH3MSB)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- ETHYL LINOLENATE (UNII: T54Y8H042V)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ETHYL OLEATE (UNII: Z2Z439864Y)
- LINOLENIC ACID (UNII: 0RBV727H71)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- LOCUST BEAN GUM (UNII: V4716MY704)
- STEARETH-2 (UNII: V56DFE46J5)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- 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".