Otc - Active Ingredient
Ethyle Alcohol 75%
Hand Sanitizer
FDA Label NDC 55059-002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Zhe Jiang Ops Environmental Technology Co.,ltd. for the product Hand Sanitizer (NDC 55059-002). 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, use, warnings, otc - do not use, otc - when using, otc - stop use, otc - purpose, 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
Use
Pump a small amount in to your palms, then briskly and thoroughly rub hands together until dry.No water needed.
Warnings
For external use only. Flammable. Keep awayfrom fire and flame.
Otc - Do Not Use
on open skin wounds
on childern under theage of 2 months
Otc - When Using
when using this product keep out of eyes,ears.and mouth.In case of contact with eyes,rinse eyes thoroughly withwater .
Otc - Stop Use
Stop use and ask a doctor if irritation or rashoccurs.These may be signs of a serious condition.
Otc - Purpose
Antiseptic
Otc - Keep Out Of Reach Of Children
Keep out of reach of childer.if swallowed,get medical help or contact a Poison Control Center right away.
Directions
Place enough product on hands to cover allsurfaces.
Rub hands together until dry.
Supervise childernunder 6 years of age when using this product to avoid.
Other Information
Store between 59°-86 F(15°-30℃)
Avoid freezing and excessive heat above 104 F (40°C)
Inactive Ingredient
Alcohol Denat,Water,Glycerol,Car-bomer,Triethanolamine,Aloe Vera.
Package Label.Principal Display Panel
Label (Label)
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