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  4. NDC Product Code: 71352-0310 Tracys Dog Personal Lubricant 300ml

NDC 71352-0310 Tracys Dog Personal Lubricant 300ml

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 71352-0310?
  4. Tracys Dog Personal Lubricant 300ml 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:
71352-0310
Proprietary Name:
Tracys Dog Personal Lubricant 300ml
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Shenzhen Beston E-commerce Co., Ltd.
Labeler Code:
71352
Product Label ID:
7be1704f-6bb0-452b-e053-2a91aa0a1b96
Start Marketing Date: [9]
12-05-2018
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
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Product Details

What is NDC 71352-0310?

The NDC code 71352-0310 is assigned by the FDA to the product Tracys Dog Personal Lubricant 300ml which is product labeled by Shenzhen Beston E-commerce Co., Ltd.. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 71352-0310-1 5 ml in 1 bottle , 71352-0310-5 240 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 Tracys Dog Personal Lubricant 300ml?

This product is a water-based personal lubricant, for penile and/or vaginal application, intended to lubricate and moisturize, to enhance the ease and comfort of intimate sexual activity and supplement to the body's natural lubricant.Apply a small amount to genital areas. Reapply as needed or desired.

Which are Tracys Dog Personal Lubricant 300ml UNII Codes?

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

Which are Tracys Dog Personal Lubricant 300ml 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".