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  4. NDC Product Code: 64483-001 Elastology Age Blocker

NDC 64483-001 Elastology Age Blocker

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 64483-001?
  5. Elastology Age Blocker Uses
  6. Active Ingredients UNII Codes
  7. 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:
64483-001
Proprietary Name:
Elastology Age Blocker
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Clientele, Inc.
Labeler Code:
64483
Product Label ID:
0a98581e-419c-4053-9f07-5b48210e48a1
Start Marketing Date: [9]
08-15-2000
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)

Code Structure Chart

Product Details

What is NDC 64483-001?

The NDC code 64483-001 is assigned by the FDA to the product Elastology Age Blocker which is product labeled by Clientele, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 64483-001-01 1 jar in 1 box / 34 g in 1 jar. 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 Elastology Age Blocker?

Apply generously 30 minutes before sun exposure and as neededChildren under 6 months of age: ask a doctorReapply as needed or after towel drying, swimming or sweating

Which are Elastology Age Blocker UNII Codes?

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

Which are Elastology Age Blocker 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".