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NDC 70465-0010 Ramosu The Witches Cream Pack Gold

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 70465-0010?
  4. Ramosu The Witches Cream Pack Gold 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:
70465-0010
Proprietary Name:
Ramosu The Witches Cream Pack Gold
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Ramosu
Labeler Code:
70465
Product Label ID:
2b00baa5-9bee-26c2-e054-00144ff8d46c
Start Marketing Date: [9]
02-04-2016
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 70465-0010-1

Package Description: 55 g in 1 PACKAGE

Product Details

What is NDC 70465-0010?

The NDC code 70465-0010 is assigned by the FDA to the product Ramosu The Witches Cream Pack Gold which is product labeled by Ramosu. The product's dosage form is . The product is distributed in a single package with assigned NDC code 70465-0010-1 55 g in 1 package . 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 Ramosu The Witches Cream Pack Gold?

Mix 01 with 02 and apply proper amount to the skin. after 15 minutes, remove it

Which are Ramosu The Witches Cream Pack Gold UNII Codes?

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

Which are Ramosu The Witches Cream Pack Gold 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".