NDC 73020-040 Papa Recipe Bombee Brightening Honey Mask Pack

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:
73020-040
Proprietary Name:
Papa Recipe Bombee Brightening Honey Mask Pack
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Costory Co., Ltd
Labeler Code:
73020
Start Marketing Date: [9]
03-01-2019
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 73020-040-02

Package Description: 10 POUCH in 1 CARTON / 25 g in 1 POUCH (73020-040-01)

Product Details

What is NDC 73020-040?

The NDC code 73020-040 is assigned by the FDA to the product Papa Recipe Bombee Brightening Honey Mask Pack which is product labeled by Costory Co., Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 73020-040-02 10 pouch in 1 carton / 25 g in 1 pouch (73020-040-01). 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 Papa Recipe Bombee Brightening Honey Mask Pack?

Directions■ Start with a dry, cleansed face.■ Remove from sachet and gently unfold and carefully place mask over the entire face, smoothing to fit the curves of the face and around eyes, nose, and mouth.■ Leave on for 10 to 20 minutes, as desired.■ Gently remove mask and lightly massage any remaining liquid into your skin, or wipe off. Do not rinse.■ Discard the mask after a single use.

Which are Papa Recipe Bombee Brightening Honey Mask Pack UNII Codes?

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

Which are Papa Recipe Bombee Brightening Honey Mask Pack 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".