Quik Spray
FDA Label NDC 41900-500

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Cinogen Cosmetics Zhaoqing, Ltd. for the product Quik Spray (NDC 41900-500). 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 otc - active ingredient, otc - purpose, warnings, dosage & administration, inactive ingredient, description, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Otc - Active Ingredient

Drug Facts

Active Ingredients                              Purpose

Ethyl Alcohol 62 percent                   Antimicrobial

Triclosan 0.3 percent                        Antimicrobial

Otc - Purpose

Uses

For hand washing to decrease bacteria on the skin,

recommended for repeated use.

Warnings

Warnings

For external use on the hands only. Flammable.

Keep away from heat and flame. Keep out if reach of children.

Stop use and ask doctor if irritation develops.

Dosage & Administration

Directions

Wet hands thoroughly with product and allow to dry without wiping.

Not recommended for infants.

Inactive Ingredient

Aloe Barbadensis Extract , Deionized Water ,  Hydroxyehylcellulose , PEG  40 Hydrogenated Castor Oil ,

Perfume , Propylene Glycol , Tocopherol

Description

Net Wt 8mL 0.27 FL OZ Made in China

Dist by Nupak, LLC 5823 Bowen Daniek Dr. 1601 Tampa FL 33616 1 888 988 7232

Package Label.Principal Display Panel

6 Hour Germ Protection

QuikSpray

90 plus sprays

Advanced Hand Sanitizing Spray

www.myquikspray.net

Contains Aloes Vera and Vitamin E

Kills 99.99 percent of germs

Quikspray24pieces (Cinogen 24 Per Box)

Quikspray24pieces (Cinogen 24 Per Box)

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