Panrosa Alcohol Free Hand Sanitizer Aloe Vera
FDA Label NDC 50302-005

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Panrosa Enterprises, Inc. for the product Panrosa Alcohol Free Hand Sanitizer Aloe Vera (NDC 50302-005). 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 ingredients, purpose, uses, warnings, do not use, when using this product,, stop use and ask a doctor if, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Active Ingredients

Benzalkonium Chloride 0.13%

Purpose

Antibacterial

Uses

  • hand sanitizer to help decrease bacteria on the skin. when water, soap & towel are not available. 
  • recommended for repeated use.

Warnings

For external use only.

Flammable. Keep away from fire or flame.

Do not apply around eyes.

Do Not Use

in ears & mouth.

When Using This Product,

avoid contact with eyes. In case of contact flush eyes with water.

Stop Use And Ask A Doctor If

redness or irritation develop and persist for more than 72 hours.

Keep Out Of Reach Of Children.

Children must be supervised in use of this product.

Directions

  • pump as need into your palms and thoroughly spread on both hands.
  • rub into skin until dry.

Other Information

  • store at 20°C (68°F to 77°F).
  • may dscolor fabrics.

Inactive Ingredients

Water, Cetrimonium Chloride, Lauramine Oxide, Cocamide Methyl MEA, Sodium Chloride, Propanediol, Parfum (Fragrance), Aloe Barbadensis Leaf Juice, Methylchloroisothiazolinone, Methylisothiazolinone, FD&C blue No. 1, FD&C yellow No. 5. 

Package Labeling:

Label3 (Label3)

Label3 (Label3)

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