NDC 71942-103 Transparent Mineral Sunscreen Facestick Broad Spectrum Spf 50

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:
71942-103
Proprietary Name:
Transparent Mineral Sunscreen Facestick Broad Spectrum Spf 50
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Amavara, Inc
Labeler Code:
71942
Start Marketing Date: [9]
02-12-2018
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 71942-103-01

Package Description: 16.8 g in 1 BOX

Product Details

What is NDC 71942-103?

The NDC code 71942-103 is assigned by the FDA to the product Transparent Mineral Sunscreen Facestick Broad Spectrum Spf 50 which is product labeled by Amavara, Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 71942-103-01 16.8 g in 1 box . 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 Transparent Mineral Sunscreen Facestick Broad Spectrum Spf 50?

This product is used as UsesHelps Prevent SunburnHigher SPF gives more sunburn protectionIf used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun.Retains SPF after 80 minutes activity in the water, sweating, or perspiring.Provides high Protection against sunburn.

Which are Transparent Mineral Sunscreen Facestick Broad Spectrum Spf 50 UNII Codes?

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

Which are Transparent Mineral Sunscreen Facestick Broad Spectrum Spf 50 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:

* Please review the disclaimer below.

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".