Package Label.Principal Display Panel
Label For Foaming (92908dymonlol)
Scrubs Foaming Hand Sanitizer
FDA Label NDC 51239-1929
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Itw Dymon for the product Scrubs Foaming Hand Sanitizer (NDC 51239-1929). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding package label.principal display panel, otc - active ingredient, otc - stop use, otc - keep out of reach of children, otc - when using, otc - purpose, otc - questions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Active Ingredient
Active Ingredients Purpose
n-alkyl dimethyl benzyl ammonium chloride (0.1%)....................................Antiseptic
n-alkyl dimethyl ethyl benzyl ammonium chloride (0.1%)..........................Antiseptic
Otc - Stop Use
Stop use and ask a doctor
- if irritation arises and persists for more than 72 hours
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Otc - When Using
When using this product
- do not get into eyes. If contact occurs rinse eyes thoroughly with water.
- Wet hands thoroughly with product and allow to dry without wiping.
- Children under six years of age should be supervised when using this product.
Directions
Otc - Purpose
Uses
- For hand washing to decrease bacteria on skin.
- Recommended for repeated use.
Otc - Questions
Inactive IngredientsWater, ethanol, Mineral Oil, Isoproply Myristate, C12-C14 Sec-pareth-5
* Please review the disclaimer below.
