NDC 50544-150 Acne Wipeout Clinical Acne System

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
50544-150
Proprietary Name:
Acne Wipeout Clinical Acne System
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
50544
Start Marketing Date: [9]
06-01-2020
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
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Product Details

What is NDC 50544-150?

The NDC code 50544-150 is assigned by the FDA to the product Acne Wipeout Clinical Acne System which is product labeled by University Medical Pharmaceuticals Corp.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 50544-150-44 1 kit in 1 kit * 120 ml in 1 tube * 30 ml in 1 tube * 60 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 Wipeout Clinical Acne System?

Adults and children 12 years of age and older:Use every morning after cleansing with Acne Wipeout™ Clear Pore Oil-Free Cleanser. Apply a dime-size amount to clean skin, avoiding the eye area. Do not rinse. If bothersome dryness or irritation occurs, reduce frequency of use. Adults and children 12 years of age and older:Use every morning and evening. Apply to damp skin and gently massage, avoiding the eye area. Rinse well. If bothersome dryness or irritation occurs, reduce frequency of use. Use only at night. Apply to face after cleansing with Acne Wipeout™ Clear Pore Oil-Free Cleanser. Do not rinse. Limit sun exposure, and use sunscreen when going outdoors. Formulated to minimize irritation. If any irritation occurs, reduce frequency of use. 

Which are Acne Wipeout Clinical Acne System UNII Codes?

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

Which are Acne Wipeout Clinical Acne System 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:

What is the NDC to RxNorm Crosswalk for Acne Wipeout Clinical Acne System?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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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".