Active Ingredient
Alcohol 80% (V/V)
One Drop Care Hand Sanitizer
FDA Label NDC 73931-012
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Guangdong Essence Daily Chemical Co., Ltd for the product One Drop Care Hand Sanitizer (NDC 73931-012). 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 active ingredient, purpose, use, warnings, keep out of reach of children., inactive ingredients, packaging, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Use
health care personnel hand rub to help reduce bacteria that potentially can cause disease.
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 mout. In case of contact, rinse eyes thoroughly with water.
Stop use and ask a doctor if
irritation or rash occurs. 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.
Inactive Ingredients
Glycerin, hydrogen peroxide, purified water USP
* Please review the disclaimer below.
