One Drop Care Hand Sanitizer
FDA Label NDC 73931-008

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 73931-008). 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., directions, inactive ingredients, packaging, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Alcohol 80% (V/V)

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.

Directions

  • Place enough product on hands to cober all survaces. Rub hands together until dry
  • Supervise children under 6 years of age when using this product to avoid swallowing.

Inactive Ingredients

Glycerin, hydrogen peroxide, purified water USP

* Please review the disclaimer below.