Otc - Active Ingredient
Ethyl Alcohol 75%
Dermarite Antibacterial Wet Wipes
FDA Label NDC 79770-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Shaoxing Hengsheng New Material Technology Development Co., Ltd. for the product Dermarite Antibacterial Wet Wipes (NDC 79770-001). 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 otc - active ingredient, otc - purpose, use, warning, otc - keep out of reach of children, directions, inactive ingredients, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
antiseptic
Use
For hand sanitizing to decrease bacteria on the skin
Warning
For external use only
Do not use in or contact the eyes
This wipes are meant for general cleaning
This wipes do not rep lace wipes used for medical procedures
keep this out of reach of children.Store below 95 F(35 C)
If swallowed,get medical help or contract a Poison Control Center
immediately
Keep in a dry place away from fire
Discontinue use if irritation and redness develop.lf the condition
persists for more than 72 hours,consult a physician.
Please close the lid after dispensing to maintain purity Aicohol by
nature evaporates quickly.
Otc - Keep Out Of Reach Of Children
Keep this out of reach of children
Directions
. Wet hands thoroughly with product and allow to dry without wiping.
Inactive Ingredients
Purified Water,Glycerin,Aloe Barbadensis
extract,Phenoxyethanol,Ethylhexylglycerin,
Propylene Glycol.
* Please review the disclaimer below.
