Active Ingredient
Ethyl Alcohol 70% v/v
Alcohol Based Hand Sanitizer Total Pure
FDA Label NDC 51384-003
10 label sections · Submitted to the FDA by Botanicals Internacional S.a. De C.v. · Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Botanicals Internacional S.a. De C.v. for the product Alcohol Based Hand Sanitizer Total Pure (NDC 51384-003). 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, indications and usage, inactive ingredients, keep out of reach section, directions, when using this product, stop use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antimicrobial
Indications And Usage
- Hand Sanitizer to help reduce bacteria that potentially can cause disease.
- For use when soap and water are not available.
Inactive Ingredients
Water, Carbomer, Triethanolamine. and Glycerine
Keep Out Of Reach Section
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Directions
• Place enough product in your palm to cover hands and rub hands together briskly until dry.
• Children under 6 years of age should be surpervised when using this product.
When Using This Product
When using this product
Do not use near or in the eyes.
In case of contact, rinse eyes thoroughly with water.
Stop Use
Stop use and ask a doctor if irritation or rash appears and lasts.
Warnings
Flammable
Keep away from heat or flame.
For external use only.
Principal Display Panel
500ML NDC: 51384-003-002
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