Active Ingredient [S]
Alcohol 75% v/v
Dr. Disin Hand Sanitizer
FDA Label NDC 79205-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Cnf Trading Group for the product Dr. Disin Hand Sanitizer (NDC 79205-001). 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 active ingredient [s], purpose, use(s), inactive ingredients:, warnings:, do not use:, when using this product:, stop use and ask a doctor:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Use(S)
Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.
Inactive Ingredients:
Purified water, Glycerin, Aloe Barbadensis Leaf Juice, Tea Tree Oil, Carbomer
Warnings:
For external use only. Flammable, keep away from heat or flame.
Do Not Use:
In children less than 2 months of age. On open skin wounds.
When Using This Product:
Keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop Use And Ask A Doctor:
If irritation or rash occur, These may be signs of a serious condition.
Keep Out Of Reach Of Children:
If swallowed, get medical help or contact a Poison Control Center right away.
Directions:
Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing.
Other Information:
Store between 15-30°C (59-86°F).
Avoid freezing and excessive heat above 40°C (104°F).
Package Labeling:
Bottle3 (Bottle3)
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