1. Labeler Index
  2. Bath & Body Works, Inc.
  3. NDC Product Code: 62670-5983 Anti-bacterial Hand Copacabana Coconut

NDC 62670-5983 Anti-bacterial Hand Copacabana Coconut

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

    1. Product Information
    2. Product Packages
    3. What is NDC 62670-5983?
    4. Anti-bacterial Hand Copacabana Coconut 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:
62670-5983
Proprietary Name:
Anti-bacterial Hand Copacabana Coconut
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Bath & Body Works, Inc.
Labeler Code:
62670
Product Label ID:
019468c3-c8cd-45dc-bc66-78200e7146c4
Start Marketing Date: [9]
12-14-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 62670-5983-0

Package Description: 29 mL in 1 BOTTLE

NDC Code 62670-5983-1

Package Description: 73 mL in 1 BOTTLE

NDC Code 62670-5983-3

Package Description: 236 mL in 1 BOTTLE, PUMP

Product Details

What is NDC 62670-5983?

The NDC code 62670-5983 is assigned by the FDA to the product Anti-bacterial Hand Copacabana Coconut which is product labeled by Bath & Body Works, Inc.. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 62670-5983-0 29 ml in 1 bottle , 62670-5983-1 73 ml in 1 bottle , 62670-5983-3 236 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 Anti-bacterial Hand Copacabana Coconut?

Rub a dime sized drop into hands.

Which are Anti-bacterial Hand Copacabana Coconut UNII Codes?

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

Which are Anti-bacterial Hand Copacabana Coconut 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".