Active Ingredient
Ethyl Alcohol 75%
Hand Sanitizer
FDA Label NDC 74881-006
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Huizhou Baozi Biotechnology Co., Ltd. for the product Hand Sanitizer (NDC 74881-006). 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, otc - do not use, when using this product, 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
Antimicrobial
Uses
Helps reduce bacteria on the s k in
Warnings
Flammable Keep awayfromfireorflame. For external use only.
Otc - Do Not Use
When using this product do not use in or near the eyes
When Using This Product
When using this product do not use in or near the eyes. Incase of contact, rinese eyes thoroughly with water, Stop use and ask doctor if irritation or rash appears and lasts, Keep out of reach for children. If swallowed , get medical help or contact a Poison Control Center right away.
Otc - Stop Use
stop use and ask a doctor if imitation or rash appears and lasts.
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
Directions: Place enough product in your palm to thoroughly spread on both hands and rub into the skin until dry
Children under 6 years of age should be supervised when using this product
Other Information
Store below 106F(41C).May discolor certain fabnics orsurfaces
Inactive Ingredients
nactive Ingredients: water, carbomer, triethanolamine
Package Label - Principal Display Panel
500 (500ml)
* Please review the disclaimer below.
