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  4. NDC Product Code: 70367-003 Acne Vanishing Gel- 10% With Sulfur

NDC 70367-003 Acne Vanishing Gel- 10% With Sulfur

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 70367-003?
  5. Acne Vanishing Gel- 10% With Sulfur 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:
70367-003
Proprietary Name:
Acne Vanishing Gel- 10% With Sulfur
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Only Yourx, Inc.
Labeler Code:
70367
Product Label ID:
270814fa-0107-6262-e054-00144ff8d46c
Start Marketing Date: [9]
03-28-2014
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Product Packages

NDC Code 70367-003-01

Package Description: 30 mL in 1 TUBE

NDC Code 70367-003-04

Package Description: 120 mL in 1 TUBE

Product Details

What is NDC 70367-003?

The NDC code 70367-003 is assigned by the FDA to the product Acne Vanishing Gel- 10% With Sulfur which is product labeled by Only Yourx, Inc.. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 70367-003-01 30 ml in 1 tube , 70367-003-04 120 ml 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 Acne Vanishing Gel- 10% With Sulfur?

Treats acne and helps prevent new blemishes from formingKills acne bacteria

Which are Acne Vanishing Gel- 10% With Sulfur UNII Codes?

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

Which are Acne Vanishing Gel- 10% With Sulfur 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".