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  4. NDC Product Code: 42952-201 I-max Lightening 5

NDC 42952-201 I-max Lightening 5

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 42952-201?
  4. I-max Lightening 5 Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
42952-201
Proprietary Name:
I-max Lightening 5
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Maxlife Usa, Inc.
Labeler Code:
42952
Product Label ID:
e874f160-1f05-4f53-8e41-8d41c2b441d8
Start Marketing Date: [9]
09-18-2012
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
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Product Details

What is NDC 42952-201?

The NDC code 42952-201 is assigned by the FDA to the product I-max Lightening 5 which is product labeled by Maxlife Usa, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 42952-201-12 59 g in 1 tube . 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 I-max Lightening 5?

USES:FOR THE GRADUAL FADING OF DARK AREAS OF THE SKIN.

Which are I-max Lightening 5 UNII Codes?

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

Which are I-max Lightening 5 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 I-max Lightening 5?

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".