Otc - Active Ingredient
Active Ingredient:
Benzalkonium Chloride 0.1%
Ultracruz Antibacterial Hand
FDA Label NDC 49877-012
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Cixi Zhixin Bird Clean-care Product Co., Ltd. for the product Ultracruz Antibacterial Hand (NDC 49877-012). 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 otc - active ingredient, otc - purpose, indications & usage, warnings, otc - stop use, otc - keep out of reach of children, dosage & administration, other safety information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Purpose:
Antiseptic
Indications & Usage
Uses:
For hand washing to kill bacterial on the skin
Warnings
Warnings
For external use only
Flammable. Keep away from fire or flame
Do not apply around eyes. Do not use in ears & mouth
When using this product, avoid contatc with eyes. In case of contact, flush eyes with water
Otc - Stop Use
Stop use and see a doctor if irritation or redness develop and persist for more than 72 hours
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. Children must be supervised in use of this product.
Dosage & Administration
Directions:
Wet hands, apply to palms, scrub thoroughly, then rinse.
Other Safety Information
Other Information:
Store at 20C (68-77F). May discolor fabrics
Inactive Ingredient
Inactive Ingredient:
Deionized water, Sodium lauryl polyoxyehthylene ether sulfate, Sodium fatty alcohol ethyl sulfate, Cocoamidoprophyl
betaine, Carboxylmethylcellulose sodium, DMDM Hydantoin, Glycerol, Frangance
Package Label.Principal Display Panel
Label Picture (012)
* Please review the disclaimer below.
