NDC 53125-785 Soapy Hands

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  2. Superior Chemical Corporation
  3. NDC: 53125-785 Soapy Hands

NDC Product Code 53125-785

NDC CODE: 53125-785

Proprietary Name: Soapy Hands What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Non-Proprietary Name: What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

NDC 53125-785-23

Package Description: 302 g in 1 CANISTER

NDC 53125-785-29

Package Description: 617 g in 1 CANISTER

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Soapy Hands with NDC 53125-785 is a product labeled by Superior Chemical Corporation. The generic name of Soapy Hands is . The product's dosage form is and is administered via form.

Labeler Name: Superior Chemical Corporation

Dosage Form: -

Product Type: What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.
  • WATER (UNII: 059QF0KO0R)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • DIMETHICONE (UNII: 92RU3N3Y1O)
  • IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Superior Chemical Corporation
Labeler Code: 53125
Start Marketing Date: 09-04-2012 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
Listing Expiration Date: 12-31-2017 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.
Exclude Flag: I 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. Values = ‘Y’ or ‘N’.

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Soapy Hands Product Label Images

Soapy Hands Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Drug Facts Box Otc-Active Ingredient Section

Benzethonium chloride USP 0.2%

Drug Facts Box Otc-Indications & Usage Section

For hand washing to decrease bacteria on skin, only when water is not available

Drug Facts Box Otc-Warnings Section

For external use only

Drug Facts Box Otc-Purpose Section

Antiseptic

Drug Facts Box Otc-When Using Section

Do not get into eyesif contact occurs, rinse eyes thoroughly with water

Drug Facts Box Otc-Stop Use Section

Irritation and redness develop

Drug Facts Box Otc-Keep Out Of Reach Of Children Section

If swallowed, get medical help or contact a Poison Control Center right away

Drug Facts Box Otc-Dosage & Administration Section

Wet hands thoroughly with product and allow to air dry without wiping wash hands with soap and water at earliest opportunity

Drug Facts Box Otc-Inactive Ingredient Section

Water, glycerine, dimethicone, DMDM hydantoin, iodopropynl butylcarbamate, fragrance

Soapy Hands 7805 50 Pre-Moistened Wipes

780550P1060.jpg Soapy Hands 50 pre-moistened wipes

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