NDC 20151-105 Lightening High Sun Protection 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:
20151-105
Proprietary Name:
Lightening High Sun Protection Cream
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
20151
Start Marketing Date: [9]
03-29-2017
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
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Product Details

What is NDC 20151-105?

The NDC code 20151-105 is assigned by the FDA to the product Lightening High Sun Protection Cream which is product labeled by Casmara Cosmetics, Sa. The product's dosage form is . The product is distributed in a single package with assigned NDC code 20151-105-02 1 bottle, dispensing in 1 bottle, dispensing / 50 ml in 1 bottle, dispensing (20151-105-01). 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 Lightening High Sun Protection Cream?

Adults and childrens 6 months of age and over: apply generaously before sun exposure. Reapply after swiming, excessive sweating or anytime after towel drying. Children under 2 years of age or less should use sunscreen products with a minium of SPF 4children under 6 months of age, consult with a doctor

Which are Lightening High Sun Protection Cream UNII Codes?

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

Which are Lightening High Sun Protection 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".