NDC 72934-6232 141060 Hydrocortisone 0.5% / Hydroquinone 4% / Tretinoin 0.025%

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:
72934-6232
Proprietary Name:
141060 Hydrocortisone 0.5% / Hydroquinone 4% / Tretinoin 0.025%
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Sincerus Florida, Llc
Labeler Code:
72934
Start Marketing Date: [9]
07-02-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
YELLOW (C48330)

Product Packages

NDC Code 72934-6232-2

Package Description: 30 g in 1 BOTTLE, PUMP

Product Details

What is NDC 72934-6232?

The NDC code 72934-6232 is assigned by the FDA to the product 141060 Hydrocortisone 0.5% / Hydroquinone 4% / Tretinoin 0.025% which is product labeled by Sincerus Florida, Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 72934-6232-2 30 g in 1 bottle, pump . 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.

Which are 141060 Hydrocortisone 0.5% / Hydroquinone 4% / Tretinoin 0.025% 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".