NDC 82665-0001 Bqcell Revirgin Gung

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:
82665-0001
Proprietary Name:
Bqcell Revirgin Gung
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
82665
Start Marketing Date: [9]
04-09-2022
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
YELLOW (C48330)
Shape:
ROUND (C48348)
Size(s):
10 MM
Imprint(s):
NONE
Score:
1

Code Structure Chart

Product Details

What is NDC 82665-0001?

The NDC code 82665-0001 is assigned by the FDA to the product Bqcell Revirgin Gung which is product labeled by Dermabqcell Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 82665-0001-1 1 tablet 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 Bqcell Revirgin Gung?

1. Cut the pouch and take out the pill-like contents. 2. Dissolve 1 pill in 50cc of water and use it as if massaging around the vulva. 3. When using it for the first time, it is recommended to use it every day for 2-3 days. After that, it is recommended to use once a week on average (except during pregnancy and menstrual period) 4. The effect is better if you learn the proper usage and cycle according to individual differences.

Which are Bqcell Revirgin Gung UNII Codes?

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

Which are Bqcell Revirgin Gung 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".