NDC 82750-001 Water Guard Slightly Acidic Electrolyzed Hypochlorous Acid Water 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:
82750-001
Proprietary Name:
Water Guard Slightly Acidic Electrolyzed Hypochlorous Acid Water Disinfectant
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
82750
Start Marketing Date: [9]
05-21-2022
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
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Product Characteristics

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Product Details

What is NDC 82750-001?

The NDC code 82750-001 is assigned by the FDA to the product Water Guard Slightly Acidic Electrolyzed Hypochlorous Acid Water Disinfectant which is product labeled by Shanghai Fuqiang-want Sanitary Accessories Co., Ltd. The product's dosage form is . The product is distributed in 4 packages with assigned NDC codes 82750-001-01 30 ml in 1 bottle , 82750-001-02 80 ml in 1 bottle , 82750-001-03 500 ml in 1 bottle , 82750-001-04 5000 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 Water Guard Slightly Acidic Electrolyzed Hypochlorous Acid Water Disinfectant?

Water Guard is mild,safe and non-irrtant. Suitable for children and pregnant women. Convenient to use with no harmful residue and no rinse needed. Gentle on skin and can be used frequently. Quick cleanse:no fragrance,no alcohol nor bleach added.

Which are Water Guard Slightly Acidic Electrolyzed Hypochlorous Acid Water Disinfectant UNII Codes?

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

Which are Water Guard Slightly Acidic Electrolyzed Hypochlorous Acid Water 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".