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  4. NDC Product Code: 76214-009 Lemon Ginger Tea Deodorant

NDC 76214-009 Lemon Ginger Tea Deodorant

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 76214-009?
  4. Lemon Ginger Tea Deodorant 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:
76214-009
Proprietary Name:
Lemon Ginger Tea Deodorant
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Skinfood Co., Ltd.
Labeler Code:
76214
Product Label ID:
4b6f59d0-f677-4af7-8372-8df2270b8a8a
Start Marketing Date: [9]
03-01-2011
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
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Product Details

What is NDC 76214-009?

The NDC code 76214-009 is assigned by the FDA to the product Lemon Ginger Tea Deodorant which is product labeled by Skinfood Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 76214-009-01 100 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 Lemon Ginger Tea Deodorant?

Indication and usage:Shake well before use. Spray on the under-arm area for 2 seconds from at least 15cm distance.

Which are Lemon Ginger Tea Deodorant UNII Codes?

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

Which are Lemon Ginger Tea Deodorant 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".