Otc - Active Ingredient
Active Ingredients - Ethyl Alcohol 70%
Lavender
FDA Label NDC 71020-012
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Sante Manufacturing Inc for the product Lavender (NDC 71020-012). 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 otc - active ingredient, otc - purpose, indications & usage, warnings, other safety information, 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
Otc - Purpose
Purpose - Antiseptic
Indications & Usage
Use
Use hand sanitizer to help reduce disease causing bacteria on the skin
Warnings
Warnings
Flammable. Keep away from fire or flame
Other Safety Information
For external use only -
Otc - When Using
Avoid contact with eyes. In case of contact, rinse eyes thoroughly with water
Otc - Stop Use
Stop use and ask a doctor if irritation or redness develops
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
Dosage & Administration
Directions
- apply liberally to hands and rub thoroughly until dry
- supervise children in teh use of this product
Inactive Ingredient
Water, Carbomer, Triethanolamine, Glycerin, Propylene Glycol, Lavandula Angustifolia Flower / Leaf / Steam Extract, Fragrance, D&C Red#33, FD&C Blue # 1
Package Label.Principal Display Panel
SpaSoap
Hand Sanitizer
Lavender
2oz / 59ml
* Please review the disclaimer below.
