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  4. NDC Product Code: 69015-100 Ultimate Aqua Blanc Protective

NDC 69015-100 Ultimate Aqua Blanc Protective

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 69015-100?
  4. Ultimate Aqua Blanc Protective Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
69015-100
Proprietary Name:
Ultimate Aqua Blanc Protective
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Racinne (hong Kong) Limited
Labeler Code:
69015
Product Label ID:
fe06a496-9627-49f7-820d-7d3eb7d30b79
Start Marketing Date: [9]
04-01-2014
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 69015-100-01

Package Description: 50 mL in 1 CARTON

Product Details

What is NDC 69015-100?

The NDC code 69015-100 is assigned by the FDA to the product Ultimate Aqua Blanc Protective which is product labeled by Racinne (hong Kong) Limited. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69015-100-01 50 ml in 1 carton . 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 Ultimate Aqua Blanc Protective?

Indications and usage:After cleansing and toning regimen, apply a small amount onto face and neck area before exposing to outdoor sunlight, avoiding eye area.For optimal results, use after Ultimate Aqua Blanc Concentrate for an enhanced brightened complexion.

Which are Ultimate Aqua Blanc Protective UNII Codes?

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

Which are Ultimate Aqua Blanc Protective 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".