NDC 80449-400 Sweat Mineral Foundation Spf 30 Shade 400

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:
80449-400
Proprietary Name:
Sweat Mineral Foundation Spf 30 Shade 400
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Sweat Cosmetics, Inc.
Labeler Code:
80449
Start Marketing Date: [9]
06-08-2015
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 80449-400-01

Package Description: 1 CONTAINER in 1 BOX / 2.7 g in 1 CONTAINER

NDC Code 80449-400-02

Package Description: 1 CONTAINER in 1 BOX / 2.7 g in 1 CONTAINER

NDC Code 80449-400-03

Package Description: 1 JAR in 1 BOX / 12 g in 1 JAR

Product Details

What is NDC 80449-400?

The NDC code 80449-400 is assigned by the FDA to the product Sweat Mineral Foundation Spf 30 Shade 400 which is product labeled by Sweat Cosmetics, Inc.. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 80449-400-01 1 container in 1 box / 2.7 g in 1 container, 80449-400-02 1 container in 1 box / 2.7 g in 1 container, 80449-400-03 1 jar in 1 box / 12 g in 1 jar. 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 Sweat Mineral Foundation Spf 30 Shade 400?

Apply generously and uniformly 15 minutes before sun exposure. Reapply after 80 minutes of swimming or sweating, or at least every 2 hours. Children under 6 months of age: ask a doctor. Avoid inhaling while applying the product.

Which are Sweat Mineral Foundation Spf 30 Shade 400 UNII Codes?

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

Which are Sweat Mineral Foundation Spf 30 Shade 400 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".