NDC 70663-010 Melano Out Mask
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 70663-010?
What are the uses for Melano Out Mask?
Which are Melano Out Mask UNII Codes?
The UNII codes for the active ingredients in this product are:
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERIN (UNII: PDC6A3C0OX) (Active Moiety)
- ALLANTOIN (UNII: 344S277G0Z)
- ALLANTOIN (UNII: 344S277G0Z) (Active Moiety)
- MINERAL OIL (UNII: T5L8T28FGP)
- MINERAL OIL (UNII: T5L8T28FGP) (Active Moiety)
Which are Melano Out Mask 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:
- SORBITOL (UNII: 506T60A25R)
- ISOHEXADECANE (UNII: 918X1OUF1E)
- WATER (UNII: 059QF0KO0R)
- LACTIC ACID (UNII: 33X04XA5AT)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- APRICOT KERNEL OIL PEG-6 ESTERS (UNII: DRG3KJZ1TJ)
- UREA HYDROCHLORIDE (UNII: RCE1061F6A)
- AZELAIC ACID (UNII: F2VW3D43YT)
- ISOSTEARYL ALCOHOL (UNII: Q613OCQ44Y)
- SODIUM LACTATE (UNII: TU7HW0W0QT)
- ARBUTIN (UNII: C5INA23HXF)
- PROPANEDIOL (UNII: 5965N8W85T)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- SODIUM ACRYLATE (UNII: 7C98FKB43H)
- SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- ENOXOLONE (UNII: P540XA09DR)
- FYTIC ACID (UNII: 7IGF0S7R8I)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- KOJIC ACID (UNII: 6K23F1TT52)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- SODIUM CETOSTEARYL SULFATE (UNII: 7ZBS06BH4B)
- SERINE (UNII: 452VLY9402)
- TRIETHANOLAMINE LACTATE (UNII: 064C51N81O)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- SALICYLIC ACID (UNII: O414PZ4LPZ)
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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".