NDC 78343-001 Plus Cosmetica S A

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:
78343-001
Proprietary Name:
Plus Cosmetica S A
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Plus Cosmetica S.a.
Labeler Code:
78343
Start Marketing Date: [9]
06-01-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 78343-001-01

Package Description: 100 mL in 1 BOTTLE, WITH APPLICATOR

Product Details

What is NDC 78343-001?

The NDC code 78343-001 is assigned by the FDA to the product Plus Cosmetica S A which is product labeled by Plus Cosmetica S.a.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 78343-001-01 100 ml in 1 bottle, with applicator . 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 Plus Cosmetica S A?

Directions: Place enough product in your palm to thoroughly cover your hands and arms. Rub hands together briskly until dry. Children under 6 years of age should be supervised when using this product.

Which are Plus Cosmetica S A UNII Codes?

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

Which are Plus Cosmetica S A 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".