NDC 70663-009 Hydraface
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 70663-009?
What are the uses for Hydraface?
Which are Hydraface UNII Codes?
The UNII codes for the active ingredients in this product are:
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERIN (UNII: PDC6A3C0OX) (Active Moiety)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
Which are Hydraface 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:
- GLYCERYL LINOLENATE (UNII: SGB6X4G86K)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- DECYL OLEATE (UNII: ZGR06DO97T)
- STEARETH-21 (UNII: 53J3F32P58)
- SORBITOL (UNII: 506T60A25R)
- STEARETH-2 (UNII: V56DFE46J5)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- WATER (UNII: 059QF0KO0R)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- SODIUM LACTATE (UNII: TU7HW0W0QT)
- SERINE (UNII: 452VLY9402)
- IMIDUREA (UNII: M629807ATL)
- TRIETHANOLAMINE LACTATE (UNII: 064C51N81O)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- LACTIC ACID (UNII: 33X04XA5AT)
- ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8)
- MIMOSA TENUIFLORA LEAF (UNII: 46VJM10Q45)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- LINALOOL, (+)- (UNII: F4VNO44C09)
- PEG-30 GLYCERYL LINOLEATE (UNII: UPJ8VI2ZOC)
- GLYCERYL ARACHIDONATE (UNII: I4WS2B978B)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- PERFLUNAFENE (UNII: 54A06VV62N)
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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".