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  4. NDC Product Code: 72197-015 Pharmacys Prescription 8 Oz Acne Control

NDC 72197-015 Pharmacys Prescription 8 Oz Acne Control

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 72197-015?
  4. Pharmacys Prescription 8 Oz Acne Control 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:
72197-015
Proprietary Name:
Pharmacys Prescription 8 Oz Acne Control
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
American Consumer Products Corp
Labeler Code:
72197
Product Label ID:
914a2512-8a3a-7771-e053-2a95a90a72e3
Start Marketing Date: [9]
09-16-2019
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 72197-015-08

Package Description: 236.58 mL in 1 BOTTLE

Product Details

What is NDC 72197-015?

The NDC code 72197-015 is assigned by the FDA to the product Pharmacys Prescription 8 Oz Acne Control which is product labeled by American Consumer Products Corp. The product's dosage form is . The product is distributed in a single package with assigned NDC code 72197-015-08 236.58 ml in 1 bottle . 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 Pharmacys Prescription 8 Oz Acne Control?

Directions: Wash face as you normally would and pat dry with a clean towel. Apply a small amount to cotton ball or pad and applyu using a dabbing motion. Take care to avoid rubbing in eyes. Use astringent two to three times daily or as directed by your doctor to keep your skin clear and healthy. Apply a light moisturizer after using astringent.

Which are Pharmacys Prescription 8 Oz Acne Control UNII Codes?

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

Which are Pharmacys Prescription 8 Oz Acne Control 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".