Active Ingredient(S)
Alcohol 75% v/v. Purpose: Antiseptic
Suppress Hand Sanitizer
FDA Label NDC 74913-610
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Shantou S.e.z Baojie Industry Co., Ltd for the product Suppress Hand Sanitizer (NDC 74913-610). 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
To decrease bacteria and other microbes
Warnings
For external use only. Flammable. Keep away from heat or flame
Do Not Use
- in children less than 2 months of age
- on open skin wounds
Otc - When Using
When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Otc - Stop Use
Stop use and ask a physician if skin irritation occurs.
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
Apply to hands thoroughly and rub vigorously until dry
For children under 6 years, use only with adult
supervision. Not recommended for infants.
Other Information
do not store above 104° F
■ may discolor some fabrics ■ harmful to some wood
finishes.
Inactive Ingredients
Water,Peg-40 hydrogenated, Castor oil, Carbomer,Sodium hydroxide, aloe vera extract
Description
Distributed by: HD Group LLC 335 N Edgewood Ln, Suite 130 Eagle, ID 83616
* Please review the disclaimer below.
