NDC 53125-785 Soapy Hands
NDC Product 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.
NDC Code Structure
- 53125 - Superior Chemical Corporation
- 53125-785 - Soapy Hands
NDC 53125-785-23
Package Description: 302 g in 1 CANISTER
NDC 53125-785-29
Package Description: 617 g in 1 CANISTER
NDC Product Information
Soapy Hands with NDC 53125-785 is a product labeled by Superior Chemical Corporation. The product's dosage form is and is administered via form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 1043330.
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 - INACTIVATED, the listing data was inactivated by the FDA. 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".
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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
- Drug Facts Box Otc-Indications & Usage Section
- Drug Facts Box Otc-Warnings Section
- Drug Facts Box Otc-Purpose Section
- Drug Facts Box Otc-When Using Section
- Drug Facts Box Otc-Stop Use Section
- Drug Facts Box Otc-Keep Out Of Reach Of Children Section
- Drug Facts Box Otc-Dosage & Administration Section
- Drug Facts Box Otc-Inactive Ingredient Section
- Soapy Hands 7805 50 Pre-Moistened Wipes
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
* Please review the disclaimer below.
