NDC 76993-0001 Joycare

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
76993-0001
Proprietary Name:
Joycare
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Joybio Corporation Agricultural Company Ltd
Labeler Code:
76993
Start Marketing Date: [9]
05-07-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 76993-0001-1

Package Description: 500 mL in 1 BOTTLE

NDC Code 76993-0001-2

Package Description: 200 mL in 1 BOTTLE

NDC Code 76993-0001-4

Package Description: 100 mL in 1 BOTTLE

NDC Code 76993-0001-5

Package Description: 120 mL in 1 BOTTLE

Product Details

What is NDC 76993-0001?

The NDC code 76993-0001 is assigned by the FDA to the product Joycare which is product labeled by Joybio Corporation Agricultural Company Ltd. The product's dosage form is . The product is distributed in 4 packages with assigned NDC codes 76993-0001-1 500 ml in 1 bottle , 76993-0001-2 200 ml in 1 bottle , 76993-0001-4 100 ml in 1 bottle , 76993-0001-5 120 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 Joycare?

Spraying it in keeping a distance of 25cm from objectives

Which are Joycare UNII Codes?

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

Which are Joycare 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".