NDC 69299-101 Quick Dry Acne Treatment

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:
69299-101
Proprietary Name:
Quick Dry Acne Treatment
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Dr. Thrower's Skincare, Inc.
Labeler Code:
69299
Start Marketing Date: [9]
11-17-2014
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 69299-101-51

Package Description: 1 BOTTLE in 1 BOX / 30 mL in 1 BOTTLE (69299-101-11)

Product Details

What is NDC 69299-101?

The NDC code 69299-101 is assigned by the FDA to the product Quick Dry Acne Treatment which is product labeled by Dr. Thrower's Skincare, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69299-101-51 1 bottle in 1 box / 30 ml in 1 bottle (69299-101-11). 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 Quick Dry Acne Treatment?

USE EVENINGS. SHAKE TO ACTIVATEAPPLY TO CLEAN SKIN AFTER SPF 30 IN AM OR ALOE MOISTURIZING CREAM IN PMAPPLY DIRECTLY TO THE ACNE OR SHAVING BUMPS WITH A COTTON SWAB.ALLOW TO DRY FOR APPROXIMATELY 5-10 MINTUES AND LEAVE ON OVERNIGHT.

Which are Quick Dry Acne Treatment UNII Codes?

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

Which are Quick Dry Acne Treatment 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 Quick Dry Acne Treatment?

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".