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  4. NDC Product Code: 62032-118 Condition And Enhance Physical Uv Block Spf 32

NDC 62032-118 Condition And Enhance Physical Uv Block Spf 32

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 62032-118?
  4. Condition And Enhance Physical Uv Block Spf 32 Uses
  5. 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:
62032-118
Proprietary Name:
Condition And Enhance Physical Uv Block Spf 32
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Omp, Inc.
Labeler Code:
62032
Product Label ID:
8c206f85-3d72-4417-bb32-8a9b7d933e71
Start Marketing Date: [9]
01-01-2004
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 62032-118?

The NDC code 62032-118 is assigned by the FDA to the product Condition And Enhance Physical Uv Block Spf 32 which is product labeled by Omp, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 62032-118-36 57 g 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 Condition And Enhance Physical Uv Block Spf 32?

The gradual bleaching of hyperpigmented skin conditions such as chloasma, melasma, freckles, senile lentigines, and other unwanted areas of melanin hyperpigmentation.

What is the NDC to RxNorm Crosswalk for Condition And Enhance Physical Uv Block Spf 32?

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".