Active Ingredient
Ethyl Alcohol 70%
Tendersant Hand Sanitizer Gel
FDA Label NDC 69771-005
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Geri-gentle Corporation for the product Tendersant Hand Sanitizer (NDC 69771-005). 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, uses:, warnings:, wehn using this product, stop use and ask a doctor if, keep out of reach of children, directions:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Uses:
To decrease bacteria on the skin.
Recommended for repeated use.
Warnings:
Flammable. Keep away from fire or flame.
For external use only. Avoid contact with broken skin.
Wehn Using This Product
do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water
Stop Use And Ask A Doctor If
irritation or rash appears and lasts
more than 72 hours consult a doctor.
Keep Out Of Reach Of Children
If swallowed, get medical helps.
Directions:
Not recommended for infants
- Wet hands thoroughly with product and allow to dry without wiping
- Children under 6 years of age should be supervised when using this product.
Other Information:
Do not store above 110°F, May discolor some fabrics.
Inactive Ingredients:
Water, Aloe Barbadensis Leaf Juice, Maltodextrin, Glycerin, Propylene Glycol, Acrylates/C10-30 Alkyl Acrylate crosspolymer, Triethanolamine, Fragrance.
Package Labeling:
Label (Label)
Box (Box)
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