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  4. NDC Product Code: 81647-070 Arocell Tone Up Perfect Sun

NDC 81647-070 Arocell Tone Up Perfect Sun

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 81647-070?
  4. Arocell Tone Up Perfect Sun 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:
81647-070
Proprietary Name:
Arocell Tone Up Perfect Sun
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Ficc Co., Ltd.
Labeler Code:
81647
Product Label ID:
5c1929ed-a463-4524-9109-23bc2f92c6bc
Start Marketing Date: [9]
03-01-2021
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 81647-070-02

Package Description: 1 TUBE in 1 CARTON / 50 g in 1 TUBE (81647-070-01)

Product Details

What is NDC 81647-070?

The NDC code 81647-070 is assigned by the FDA to the product Arocell Tone Up Perfect Sun which is product labeled by Ficc Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 81647-070-02 1 tube in 1 carton / 50 g in 1 tube (81647-070-01). 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 Arocell Tone Up Perfect Sun?

■ Apply liberally and uniformly to all exposed areas 15-20 minutes before sun exposure.

Which are Arocell Tone Up Perfect Sun UNII Codes?

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

Which are Arocell Tone Up Perfect Sun 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".