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  4. NDC Product Code: 64249-0004 Momlove

NDC 64249-0004 Momlove

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 64249-0004?
  4. Momlove 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:
64249-0004
Proprietary Name:
Momlove
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Vitamed, Llc
Labeler Code:
64249
Product Label ID:
967b6a9e-c193-4fcd-8f95-cb39fa90f706
Start Marketing Date: [9]
08-18-2014
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
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Product Details

What is NDC 64249-0004?

The NDC code 64249-0004 is assigned by the FDA to the product Momlove which is product labeled by Vitamed, Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 64249-0004-1 30 ml in 1 bottle, spray . 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 Momlove?

May temporarily relieve symptoms associated with pregnancy such as morning sickness, emotional fluctuations, backaches, bladder problems and hemorrhoids. ****These statements are based upon traditional homeopathic practice. They have not been reviewed by the U.S. Food and Drug Administration. May temporarily relieve symptoms associated with pregnancy such as morning sickness, emotional fluctuations, backaches, bladder problems and hemorrhoids. ****These statements are based upon traditional homeopathic practice. They have not been reviewed by the U.S. Food and Drug Administration.

Which are Momlove UNII Codes?

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

Which are Momlove 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".