Active Ingredient
ETHYL alcohol 65% v/v. Purpose: Antiseptic
Hand Sanitizer
FDA Label NDC 75328-002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Crown (yangzhou) Health & Beauty Co., Ltd for the product Hand Sanitizer (NDC 75328-002). 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, do not use, stop use, keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic, Hand Sanitizer
Uses
- Hand Sanitizer to help reduce bacteria that potentially can cause disease.
- For use when soap and water are not available.
Warnings
For external use only. Flammable. Keep away from heat or flame.
Do Not Use
near or in the eyes. If contact occurs, rinse eyes with water throughly.
Stop Use
Stop use and ask a physician if irritation,rash, or redness develops.
Keep Out Of Reach Of Children
If swallowed get medical help or contact a Poison Control Center right away.
Directions
- Place enough product on hands to cover all surfaces. Rub hands together until dry.
- Supervise children under 6 years of age when using this product to avoid swallowing.
Other Information
- Should be stored below 110℉(43℃)
- Can discolor surfaces and some fabrics
Inactive Ingredients
deionized water, aminomethyl propanol, carbomer, propanediol, tocopheryl acetate, isopropyl myristate, glycerin, fragrance, water
Package Label - Principal Display Panel
500mL NDC: 75328-002-01
500ml Label (500ml)
946mL NDC: 75328-002-02
946ml Label (946ml)
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