NDC 70663-007 Melano Out Cream
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70663 - Meso System S.a.
- 70663-007 - Melano Out Cream
Product Packages
NDC Code 70663-007-02
Package Description: 30 CONTAINER in 1 BOX / 30 mL in 1 CONTAINER (70663-007-01)
Product Details
What is NDC 70663-007?
What are the uses for Melano Out Cream?
Which are Melano Out Cream UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALLANTOIN (UNII: 344S277G0Z)
- ALLANTOIN (UNII: 344S277G0Z) (Active Moiety)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERIN (UNII: PDC6A3C0OX) (Active Moiety)
Which are Melano Out Cream 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:
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8)
- WATER (UNII: 059QF0KO0R)
- AZELAIC ACID (UNII: F2VW3D43YT)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- MINERAL OIL (UNII: T5L8T28FGP)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- KOJIC ACID (UNII: 6K23F1TT52)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- LACTIC ACID (UNII: 33X04XA5AT)
- SODIUM LACTATE (UNII: TU7HW0W0QT)
- SORBITOL, L- (UNII: 01Q0586BG1)
- TRIETHANOLAMINE LACTATE (UNII: 064C51N81O)
- ARBUTIN (UNII: C5INA23HXF)
- ALLANTOIN GLYCYRRHETINIC ACID (UNII: H6FL381368)
- FYTIC ACID (UNII: 7IGF0S7R8I)
- SODIUM CETOSTEARYL SULFATE (UNII: 7ZBS06BH4B)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- SERINE (UNII: 452VLY9402)
- HYDROXYETHYL UREA (UNII: MBQ7DDQ7AR)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
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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".