Carricare Premium Hand Sanitizer
FDA Label NDC 74923-110

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by The Sun Co.ltd for the product Carricare Premium Hand Sanitizer (NDC 74923-110). 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, inactive ingredients, purpose, warnings, keep out of reach of children, uses, directions, package label: carricare premium hand sanitizer spray (20ml, black)ndc : 74923-110-01, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Ethyl Alcohol 70.0%

Inactive Ingredients

Glycerin, Aloe Vera Extract, Grapefruit Seeds Extract, Rosemary Extract, Green Tea Extract, and Purified Water.

Purpose

Antiseptic

Warnings

For external use only

Flammable. Keep away from heat and flame.

When using this product
■ Avoid contact with face, eyes, and broken skin.
■ In case of eyes contact, flush with plenty of water and seek medical advice.

Stop use and ask a doctor if
■ irritation or redness develops.

Keep Out Of Reach Of Children

If swallowed, get medical help or contact a Poison Control Center.

Uses

■ Hand washing to help reduce bacteria on the skin.

Directions

■ Spray hands thoroughly with product and rub in to skin until dry.
■ Children under 6 years of age should be supervised by an adult when using.
■ Not recommended for infants.

* Please review the disclaimer below.