NDC 41506-002 Elepbaby Disinfectant

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:
41506-002
Proprietary Name:
Elepbaby Disinfectant
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
41506
Start Marketing Date: [9]
04-08-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Imprint(s):
ELEPBABY

Code Structure Chart

Product Details

What is NDC 41506-002?

The NDC code 41506-002 is assigned by the FDA to the product Elepbaby Disinfectant which is product labeled by Suzhou Nagongfang Health Technology Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 41506-002-01 500 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 Elepbaby Disinfectant?

1、Use without dilution, direct spraying, 5- 10ml per square meter, 60 seconds after the completion of sterilization. 2、Spray after natural air drying, do not immediately dry water, otherwise it will reduce the disinfection effect. 3、To metal utensils, tableware, fruits, vegetables disinfection, can be directly soaked with this product,soaked for three minutes with water rinse clean. 4、Clean fibers, fur products, clothing, closets and cupboards before spraying, and repeat the spray every 3 hours for better results. 5、When disinfecting the pet, please put a good muzzle on the pet to avoid excessive licking.

Which are Elepbaby Disinfectant UNII Codes?

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

Which are Elepbaby Disinfectant 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".