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  4. NDC Product Code: 76255-2001 Letomint

NDC 76255-2001 Letomint

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 76255-2001?
  5. Letomint Uses
  6. Active Ingredients UNII Codes
  7. 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:
76255-2001
Proprietary Name:
Letomint
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
H&c 21 America Inc
Labeler Code:
76255
Product Label ID:
fe10b461-11a8-4d0b-9774-dcdbd8517953
Start Marketing Date: [9]
06-18-2011
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325 - IVORY WHITE)
Shape:
OVAL (C48345)
Size(s):
10 MM
Imprint(s):
3;HP;X
Score:
1

Code Structure Chart

Product Details

What is NDC 76255-2001?

The NDC code 76255-2001 is assigned by the FDA to the product Letomint which is product labeled by H&c 21 America Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 76255-2001-1 18 tablet in 1 box . 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 Letomint?

- if you put this into your vaginas deeply, it will show its effectsas- it melts and soaked into your skin by itself after 30~40 minutes- please make sure to check sediments by having a sitz batn- your wombs will get back to healthy of twenties if you continue to use one pill per 2~3days

Which are Letomint UNII Codes?

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

Which are Letomint 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:

* Please review the disclaimer below.

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".