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  4. NDC Product Code: 81983-101 Female Intimate Hygiene Antibacterial Gels

NDC 81983-101 Female Intimate Hygiene Antibacterial Gels

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 81983-101?
  4. Female Intimate Hygiene Antibacterial Gels Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
81983-101
Proprietary Name:
Female Intimate Hygiene Antibacterial Gels
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Shenzhen Mengti Biotechnology Co.ltd
Labeler Code:
81983
Product Label ID:
c43920ab-2925-2dd2-e053-2995a90a1df2
Start Marketing Date: [9]
06-08-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 81983-101-02

Package Description: 10 BAG in 1 BOX / 3.5 g in 1 BAG (81983-101-01)

Product Details

What is NDC 81983-101?

The NDC code 81983-101 is assigned by the FDA to the product Female Intimate Hygiene Antibacterial Gels which is product labeled by Shenzhen Mengti Biotechnology Co.ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 81983-101-02 10 bag in 1 box / 3.5 g in 1 bag (81983-101-01). 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 Female Intimate Hygiene Antibacterial Gels?

Wash hands and clean the vulvaRemove the front cover of the gel and insert the removed front cover into the rear end of the gel tube as a push rodLie on your back and push the gel into the vagina with the gel pusherTake out the gel pusher, and lie still for three minutes.

Which are Female Intimate Hygiene Antibacterial Gels UNII Codes?

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

Which are Female Intimate Hygiene Antibacterial Gels 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".