Active Ingredients
Ethyl Alcohol 75% Purpose: Antibactirial
Hand Sanitizer
FDA Label NDC 78048-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Dongguan City Dexu Toys Co.,ltd for the product Hand Sanitizer (NDC 78048-001). 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 ingredients, purpose, uses, warnings, otc - do not use, otc - when using, stop use and ask a doctor if, 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
Antibacterial
Uses
for handwashing to decrease bacteria on the skin
Warnings
Flammable. Keep away from heat or flame.For external use only.
Otc - Do Not Use
do not use in eyes.In case of contact with eye rinse with water
Otc - When Using
when using this product do not use in eyes.In case of contact with eye rinse with water
Stop Use And Ask A Doctor If
irritation or redness develop and persist
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help promiptly
Directions
Wet hands thoroughly with product and allow to dry without wiping
Other Information
Store under 105℉
Inactive Ingredients
ALOE BARBADENSIS LEAF,carbomer,dimethicone,triisopropanolamine,water
Package Label - Principal Display Panel
50mL NDC: 78048-001-01
Label (Label)
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