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  4. NDC Product Code: 69602-1001 Camelia Body

NDC 69602-1001 Camelia Body

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 69602-1001?
  4. Camelia Body 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:
69602-1001
Proprietary Name:
Camelia Body
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Saebyuck Corp.
Labeler Code:
69602
Product Label ID:
cface2a2-a040-4ff3-9ebb-a15d1c8e13ec
Start Marketing Date: [9]
03-08-2015
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 69602-1001-1

Package Description: 250 mL in 1 BOTTLE

Product Details

What is NDC 69602-1001?

The NDC code 69602-1001 is assigned by the FDA to the product Camelia Body which is product labeled by Saebyuck Corp.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69602-1001-1 250 ml in 1 bottle . 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 Camelia Body?

Towel dry your body completely after shower or bathput an appropriate amount of body lotion onto the palm of your hand and massage lotion gently to the skin

Which are Camelia Body UNII Codes?

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

Which are Camelia Body 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:

* Please review the disclaimer below.

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".