Active Ingredient(S)
Alcohol 70% v/v. Purpose: Antiseptic
Washing-free Hand Sanitizer
FDA Label NDC 74916-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Jiangxi Zhangshu Zhengkang Medicine Biotechnology Co.,ltd. for the product Washing-free Hand Sanitizer (NDC 74916-001). 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(s), purpose, use, warnings, do not use, otc - when using, otc - stop use, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic, Hand Sanitizer
Use
Hand Sanitizer to help reduce bacteria on the skin
Warnings
This product is a disinfectant for external use only. Flammable. Keep away from open flame and source of heat
Do Not Use
It is forbidden to take orally
Otc - When Using
Avoid contact with the eyes. If contact occurs, flush eyes with water.
Otc - Stop Use
Discontinue use and consult a health-care practitioner if irritation develops.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
1. Hand sanitizing: Place some product in your palm to thoroughly cover your hands. Rub hands together briskly until dry. Chirldren under 6 years of age should be supervised when using this product. Use a part of your daily cleansing routine.
2. Surgical hand antisepsis: After surgical hand washing, place some product in your hands, forearm and upper arm 1/3 skin, rub them together briskly for 3-5 minutes, then can wear sterile golves.
Other Information
- Store below 110F (43C).
- May discolor certain fabrics or surfaces
Inactive Ingredients
Water (purified), Glycerin, Grape fruit extract, Honeysuckle extract, wormwood leaf extract, Aloe extract, Carbomer, Sodium hyaluronate, Triethanolamine, Propylene glycol
Package Label - Principal Display Panel
50 mL NDC: 74621-001-01
Pdp (74916 001 01)
500 mL NDC: 74621-001-02
Pdp (74916 001 02)
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