NDC 60659-0102 Bang Er Jie High-efficiency Anti-bacteria Monomer Silver -lotion For Women

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:
60659-0102
Proprietary Name:
Bang Er Jie High-efficiency Anti-bacteria Monomer Silver -lotion For Women
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
60659
Start Marketing Date: [9]
09-22-2013
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
BROWN (C48332)

Code Structure Chart

Product Details

What is NDC 60659-0102?

The NDC code 60659-0102 is assigned by the FDA to the product Bang Er Jie High-efficiency Anti-bacteria Monomer Silver -lotion For Women which is product labeled by Bang An Bao Medical Equipment Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 60659-0102-1 200 ml in 1 bottle, plastic . 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 Bang Er Jie High-efficiency Anti-bacteria Monomer Silver -lotion For Women?

This product is used as Anti-BacteriaMonomer silver gel is a highly active agent which significantly suppresses and eliminates Candida albicans, Escherichia coli, Staphylococcus aureus and Pseudomonas aeruginosa within and around the vagina, prevents and cures inflammation, accelerates the recovery of wounds and lesioned tissues regardless of vagina pH without affecting normal vaginal bacteria.

Which are Bang Er Jie High-efficiency Anti-bacteria Monomer Silver -lotion For Women UNII Codes?

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

Which are Bang Er Jie High-efficiency Anti-bacteria Monomer Silver -lotion For Women 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".