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  4. NDC Product Code: 70907-001 Numb Skin

NDC 70907-001 Numb Skin

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 70907-001?
  4. Numb Skin 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:
70907-001
Proprietary Name:
Numb Skin
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Seenext Venture Ltd
Labeler Code:
70907
Product Label ID:
3ac18167-774b-3777-e054-00144ff8d46c
Start Marketing Date: [9]
09-01-2016
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
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Product Details

What is NDC 70907-001?

The NDC code 70907-001 is assigned by the FDA to the product Numb Skin which is product labeled by Seenext Venture Ltd. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 70907-001-15 1 tube in 1 cartridge / 15 g in 1 tube, 70907-001-30 1 tube in 1 cartridge / 30 g in 1 tube. 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 Numb Skin?

Adults: When practical, cleanse the affected area with mild soap and warm water and rinse thoroughly. Gently dry by patting or blotting with tissue or a soft cloth before application of product.when first opening the tube, puncture foil seal with top end of capapply externally to the affected area up to 6 times dailychildren under 12 years of age: consult a doctor

Which are Numb Skin UNII Codes?

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

Which are Numb Skin 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".