Tenderlaven Hand Gel
FDA Label NDC 69771-006

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 Tenderlaven Hand (NDC 69771-006). 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:, stop use:, keep out of reach of children, directions:, other information:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Active Ingredient

Chloroxylenol 0.2%

Purpose

Antiseptic

Uses:

For handwashing to decrease bacteria on the skin.

Warnings:

For external use only. Avoid contact with eyes. In case of contact, flush 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

except under adult supervision. In case of accidental ingestion contact a physician or Poison Control Center right away.

Directions:

Wet hands and forearms. Apply 5 ml (teaspoon) or palmful to hands and forearms. Scrub thoroughly for 15 seconds. Rinse and repeat.

Other Information:

Store in a cool place away from direct sunlight.

Inactive Ingredients:

Water, sodium lauryl sulfate, Cocamide DEA, Cocamidopropyl Betaine, Glycerin, Citric Acid, Sodium chloride, Disodium EDTA, fragrance, Methylchloroisothiazolinone and Methylisothiazolinone, D&C Red NO.33, FD&C Blue NO.1

Package Labeling:

Label2 (Label2)

Label2 (Label2)

Label3 (Label3)

Label3 (Label3)

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