NDC 52554-5001 Laser Rejuvenation Restoring Damage Skin

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:
52554-5001
Proprietary Name:
Laser Rejuvenation Restoring Damage Skin
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Universal Cosmetic Co., Ltd
Labeler Code:
52554
Start Marketing Date: [9]
08-19-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 52554-5001-1

Package Description: 30 mL in 1 BOTTLE, PLASTIC

Product Details

What is NDC 52554-5001?

The NDC code 52554-5001 is assigned by the FDA to the product Laser Rejuvenation Restoring Damage Skin which is product labeled by Universal Cosmetic Co., Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 52554-5001-1 30 ml in 1 bottle, plastic . 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 Laser Rejuvenation Restoring Damage Skin?

Direction■ Apply after cleansing.■ Apply appropriate amounts onto the skin defect and damaged areas and then absorb patting gently, morning and night.

Which are Laser Rejuvenation Restoring Damage Skin UNII Codes?

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

* Please review the disclaimer below.

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".