Active Ingredient
Ethyl Alcohol 64%
Yogardtm Hand Sanitizer
FDA Label NDC 78920-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Zhejiang Meijiahua Medical Technology Co., Ltd. for the product Yogardtm Hand Sanitizer (NDC 78920-001). 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 ingredient, purpose, use, warnings, 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
Purpose
Antisepic
Use
instant hand sanitizer
.suitable for disinfection of sanitary hands and surgical hands
.recommended for repeated use
Warnings
Warnings Flammable, Keep away from fire or flame.
For external use only
When using this productâ—ŹKeep out of eyes. lfcontact with eyes occurs,
rinse promptly and thoroughly with water.
Stop use and ask a doctor if significant irtation, or sensitizaion develops.
Do notuse on chronic skin conditions such as a leg ulcer ,diaper rash,or hand eczema.
Otc - Keep Out Of Reach Of Children
keep out of reach of children. If sallowed, get medical help or contact a Poison Control Center right away.
Directions
Directions Apply to clean, dry hands. Wet hands thoroughly with product and allow to dry.
Inactive Ingredients
Aqua, Glycerol, Aloe Barbadensis Extract, Tocopheryl Acetate (Vitamin E), Carbomer, Triethanolamine
Package Label.Principal Display Panel
1 (Label)
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