NDC 76348-461 Gold Mountain Beauty Drying

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:
76348-461
Proprietary Name:
Gold Mountain Beauty Drying
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Renu Laboratories, Inc.
Labeler Code:
76348
Start Marketing Date: [9]
01-04-2021
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 76348-461-02

Package Description: 1 BOTTLE, GLASS in 1 BOX / 28 mL in 1 BOTTLE, GLASS (76348-461-01)

Product Details

What is NDC 76348-461?

The NDC code 76348-461 is assigned by the FDA to the product Gold Mountain Beauty Drying which is product labeled by Renu Laboratories, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 76348-461-02 1 bottle, glass in 1 box / 28 ml in 1 bottle, glass (76348-461-01). 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 Gold Mountain Beauty Drying?

This product is used as Topical Acne Treatment. For the treatment of acnehealing and drying acne breakoutshelps clear acne pimples, blackheads or whiteheads and allows skin to healpenetrates pores to control acne blemisheshelps keep skin clear of new acne pimples

Which are Gold Mountain Beauty Drying UNII Codes?

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

Which are Gold Mountain Beauty Drying 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".