NDC 58876-106 Acne Spot Corrector Maximum Strength

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:
58876-106
Proprietary Name:
Acne Spot Corrector Maximum Strength
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Dr Lin Skincare
Labeler Code:
58876
Start Marketing Date: [9]
06-13-2013
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 58876-106-91

Package Description: 1 TUBE in 1 BOX / 30 mL in 1 TUBE (58876-106-31)

Product Details

What is NDC 58876-106?

The NDC code 58876-106 is assigned by the FDA to the product Acne Spot Corrector Maximum Strength which is product labeled by Dr Lin Skincare. The product's dosage form is . The product is distributed in a single package with assigned NDC code 58876-106-91 1 tube in 1 box / 30 ml in 1 tube (58876-106-31). 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 Spot Corrector Maximum Strength?

USEFOR THE TREATMENT OF ACNE AND ACNE DARK AND RED MARKS.

Which are Acne Spot Corrector Maximum Strength UNII Codes?

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

Which are Acne Spot Corrector Maximum Strength 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 Spot Corrector Maximum Strength?

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".