NDC 73261-0001 Bueno Salmon S.o.s Mask

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:
73261-0001
Proprietary Name:
Bueno Salmon S.o.s Mask
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Bueno Meditech
Labeler Code:
73261
Start Marketing Date: [9]
08-02-2019
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 73261-0001-1

Package Description: 40 mL in 1 POUCH

Product Details

What is NDC 73261-0001?

The NDC code 73261-0001 is assigned by the FDA to the product Bueno Salmon S.o.s Mask which is product labeled by Bueno Meditech. The product's dosage form is . The product is distributed in a single package with assigned NDC code 73261-0001-1 40 ml in 1 pouch . 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 Bueno Salmon S.o.s Mask?

After cleansing your face, apply some skin tonertake the product out of the package and adhere it evenly over your face avoiding the eye and mouth arearemove it after 10-20 minutes, using your fingers, gently pat any remaining product into the skin until thoroughly absorbedsqeeze remaining essence in pouch and apply on dried skin

Which are Bueno Salmon S.o.s Mask UNII Codes?

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

Which are Bueno Salmon S.o.s Mask 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".