NDC 70663-007 Melano Out Cream

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
70663-007
Proprietary Name:
Melano Out Cream
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Meso System S.a.
Labeler Code:
70663
Start Marketing Date: [9]
12-17-2016
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

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?

The NDC code 70663-007 is assigned by the FDA to the product Melano Out Cream which is product labeled by Meso System S.a.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 70663-007-02 30 container in 1 box / 30 ml in 1 container (70663-007-01). This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Melano Out Cream?

Clean the skin thoroughly before applying the cream.Cover the entire affected area with a thin layer. First week apply three times daily (morning-afternoon-night). Second week apply two times daily (morning-night). Third week apply once a day for one year.During summer it is recommended the application of the cream after sun exposure. If bothersome dryness or peeling occurs, reduce application to once a day or every other day

Which are Melano Out Cream UNII Codes?

The UNII codes for the active ingredients in this product are:

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:

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Product Footnotes

[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".