NDC 72798-010 La Femme V Feminine Cleanser

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:
72798-010
Proprietary Name:
La Femme V Feminine Cleanser
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Nature Factory Co., Ltd.
Labeler Code:
72798
Start Marketing Date: [9]
12-01-2018
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
OVAL (C48345)
Size(s):
15 MM
Score:
1

Product Packages

NDC Code 72798-010-02

Package Description: 5 CONTAINER in 1 CARTON / 800 mg in 1 CONTAINER (72798-010-01)

Product Details

What is NDC 72798-010?

The NDC code 72798-010 is assigned by the FDA to the product La Femme V Feminine Cleanser which is product labeled by Nature Factory Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 72798-010-02 5 container in 1 carton / 800 mg in 1 container (72798-010-01). 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 La Femme V Feminine Cleanser?

Directions: 1.Use it at bedtime preferably or during daytime without dynamic activities. 2.Wash your finger and insert 1 tablet into the vagina with first two knuckles of a finger. 3.It will take 20-30 minutes until the tablet is dissolved to relieve the symptoms and clean the vagina. 4.Do not use within 6 hours prior to vaginal intercourse.

Which are La Femme V Feminine Cleanser UNII Codes?

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

Which are La Femme V Feminine Cleanser 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".