NDC 73265-030 Voye Fresh Up Perfect Moisture Mask V Hyaluron Moisture Ampule

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:
73265-030
Proprietary Name:
Voye Fresh Up Perfect Moisture Mask V Hyaluron Moisture Ampule
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Golden Street
Labeler Code:
73265
Start Marketing Date: [9]
07-01-2019
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 73265-030-02

Package Description: 10 POUCH in 1 CARTON / 28 mL in 1 POUCH (73265-030-01)

Product Details

What is NDC 73265-030?

The NDC code 73265-030 is assigned by the FDA to the product Voye Fresh Up Perfect Moisture Mask V Hyaluron Moisture Ampule which is product labeled by Golden Street. The product's dosage form is . The product is distributed in a single package with assigned NDC code 73265-030-02 10 pouch in 1 carton / 28 ml in 1 pouch (73265-030-01). 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 Voye Fresh Up Perfect Moisture Mask V Hyaluron Moisture Ampule?

Directions:1. Fold three times the bottom of pouch along the dotted line2. Roll it after folding the pouch three times3. Mix it after shaking the mask sheet when the bubbles sink completely4. Take out the sheet and remove one side from the coverTake out the other side after putting it on the face5. Remove the mask after taking a rest for 15 – 20 minutesMake the essence absorbed to the skin by tapping it.

Which are Voye Fresh Up Perfect Moisture Mask V Hyaluron Moisture Ampule UNII Codes?

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

Which are Voye Fresh Up Perfect Moisture Mask V Hyaluron Moisture Ampule 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".