Active Ingredient(S)
Ethyl Alcohol 70% v/v. Purpose: Antimicrobial
Hand Sanitizer
FDA Label NDC 74738-1105
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 B.c. Biotech Co., Ltd. for the product Hand Sanitizer (NDC 74738-1105). 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, warnings, do not use, otc - when using, otc - stop use, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Hand Sanitizer to help reduce bactreia on skin.
Use
Hand Sanitizer to help reduce bacteria on skin.
Warnings
Flammable. Keep away from fire or flame.
For external use only.
Do Not Use
Do not use in or near the eyes.
In case of contact, rinse eyes thoroughly with water.
Otc - When Using
When using this product, do not use in or near the eyes.
Otc - Stop Use
Stop use and ask a doctor if irritation or rash appears and lasts.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
- Place enough Product in your palm to thoroughly spread on both hands and rub into the skin until dry.
- Children under 6 years of age should be supervised when using this product.
Other Information
- Store below 106℉ (41℃)
- May discolor certain fabrics or surfaces
Inactive Ingredients
Water (Aqua), Olive Oil PEG-7 Esters, Acrylates/C10-30 Alkyl, Acrylate Crosspolymer, Aminomethyl Propanol, Aloe Barbadensis Leaf Extract
* Please review the disclaimer below.
