NDC 63509-002 Skin Activator Lip Refiner Spf 15
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 63509-002?
Which are Skin Activator Lip Refiner Spf 15 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 Skin Activator Lip Refiner 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- ISOPROPYL ISOSTEARATE (UNII: C67IXB9Y7T)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- DIISOPROPYL DILINOLEATE (UNII: 5323S7S2LR)
- SHEA BUTTER (UNII: K49155WL9Y)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- SQUALANE (UNII: GW89575KF9)
- DIPALMITOYL HYDROXYPROLINE (UNII: E6AHA53N1H)
- GLUCOSAMINE HYDROCHLORIDE (UNII: 750W5330FY)
- LAMINARIA DIGITATA (UNII: 15E7C67EE8)
- YEAST (UNII: 3NY3SM6B8U)
- UREA (UNII: 8W8T17847W)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- TRIBEHENIN (UNII: 8OC9U7TQZ0)
- SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)
- PALMITOYL OLIGOPEPTIDE (UNII: HO4ZT5S86C)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
- LEVOMENOL (UNII: 24WE03BX2T)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- XANTHAN GUM (UNII: TTV12P4NEE)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PEG-100 STEARATE (UNII: YD01N1999R)
- PEPPERMINT OIL (UNII: AV092KU4JH)
- EDETATE SODIUM (UNII: MP1J8420LU)
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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".