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NDC 75397-0002 Subuni Breast Pack

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 75397-0002?
  4. Subuni Breast Pack 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:
75397-0002
Proprietary Name:
Subuni Breast Pack
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Merlin
Labeler Code:
75397
Product Label ID:
a3a14d1a-ed25-5352-e053-2a95a90a7b87
Start Marketing Date: [9]
04-04-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Product Details

What is NDC 75397-0002?

The NDC code 75397-0002 is assigned by the FDA to the product Subuni Breast Pack which is product labeled by Merlin. The product's dosage form is . The product is distributed in a single package with assigned NDC code 75397-0002-1 25 g in 1 pouch . 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 Subuni Breast Pack?

①Take out breast pack from pouch and remove one sheet from both sheets. (Same with opposite breast pack.) ②Put nipple in the center of the hole and place sheet in desired direction. ③Press sheet according to shape of breast evenly. ④Relax for 15~20 mins and make sure essence is absorbed into breast. ※ You can massage your breast after with left essence.

Which are Subuni Breast Pack UNII Codes?

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

Which are Subuni Breast Pack 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".