Active Ingredient
Alcohol 75%
Hand Sanitizer Set
FDA Label NDC 74657-004
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Double Body Biotech Limited for the product Hand Sanitizer Set (NDC 74657-004). 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, purpose, use, warnings, do not use, when using this product, keep out of reach of children, 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
Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.
Warnings
For external use only. Flammable. Keep away heat or flame.
Do Not Use
- in children less than 2 months of age
- on open skin wounds
When Using This Product
When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away.
Stop Use And Ask A Doctor
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Directions
Wet hands thoroughly with gel, rub vigorously and allow to dry without wiping. Children under 6 years of age should be supervised when using this product.
Other Information
Store below 106 F(41 C)
Inactive Ingredients
water
glycereth-26
aloe barbadensis extract,
carbomer,
sodium hydroxide,
may contain: red 33, red 4, yellow 5, blue 1, red 40.
Label
* Please review the disclaimer below.
