1. Home
  2. Labeler Index
  3. Truezyme Co., Ltd.
  4. NDC Product Code: 71076-0002 Truezyme Baby Shampooandbody Wash

NDC 71076-0002 Truezyme Baby Shampooandbody Wash

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 71076-0002?
  4. Truezyme Baby Shampooandbody Wash 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:
71076-0002
Proprietary Name:
Truezyme Baby Shampooandbody Wash
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Truezyme Co., Ltd.
Labeler Code:
71076
Product Label ID:
41652c38-145f-062b-e054-00144ff8d46c
Start Marketing Date: [9]
10-01-2016
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 71076-0002?

The NDC code 71076-0002 is assigned by the FDA to the product Truezyme Baby Shampooandbody Wash which is product labeled by Truezyme Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 71076-0002-1 300 ml in 1 bottle, pump . 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 Truezyme Baby Shampooandbody Wash?

- Wet the whole body and lather well on a shower sponge, a towel, or hands and massage the whole body gently and wash away with water cleanly.- For a bath, you can enjoy a refreshing enzymatic bath by lathering enough in warm water.* Shake well before use.

Which are Truezyme Baby Shampooandbody Wash UNII Codes?

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

Which are Truezyme Baby Shampooandbody Wash 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".