Tendersant Hand Sanitizer Gel
FDA Label NDC 69771-007

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 69771-007). 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 drug facts, active ingredient, purpose, uses:, warnings, when using this product, stop use:, 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

Drug Facts

Active Ingredient

Ethyl Alcohol 70%

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.

When Using This Product

do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water

Stop Use:

if irritation or redness develops.

  • If condition persists for more than 72 hours consult a doctor.

Keep Out Of Reach Of Children

If swallowed, get medical help

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:118Ml

Bottle (Bottle)

Bottle (Bottle)

Package Labeling:500Ml

Bottle2 (Bottle2)

Bottle2 (Bottle2)

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