NDC 50950-001 Iman Time Control All Day Moisture Complex Spf 15

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:
50950-001
Proprietary Name:
Iman Time Control All Day Moisture Complex Spf 15
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Sheencolor Biotech Co., Ltd.
Labeler Code:
50950
Start Marketing Date: [9]
08-10-2010
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 50950-001-01

Package Description: 89 g in 1 TUBE

Product Details

What is NDC 50950-001?

The NDC code 50950-001 is assigned by the FDA to the product Iman Time Control All Day Moisture Complex Spf 15 which is product labeled by Sheencolor Biotech Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 50950-001-01 89 g in 1 tube . 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 Iman Time Control All Day Moisture Complex Spf 15?

This product is used as This long lasting moisturizing complex, enriched with Vitamin E, Silk Protein, Fruit Acids, and Botanic Extracts, leaves skin soft, supple, and radiant.SPF-15 helps to protect against the harmful effect of the sun.

Which are Iman Time Control All Day Moisture Complex Spf 15 UNII Codes?

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

Which are Iman Time Control All Day Moisture Complex 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:

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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".