Active Ingredient
Ethyl Alcohol 65%
Hand Sanitizer
FDA Label NDC 51706-600
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Landy International for the product Hand Sanitizer (NDC 51706-600). 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, warning, keep out of reach of children., directions, other information, inactive ingredient, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Uses
To decrease bacteria on the skin.
Warning
For external use only.
When using this product avoid contact with eyes.In case of contact flush eyes thoroughly with water.
Flammable.
Keep away from heat and flame.
Stop use and consult a doctor
if irritation and redness develop and persist for more than 72 hours.
Keep Out Of Reach Of Children.
If swallowed,get medical help or contact Poison Control Center right away
Directions
■ Wet hands with product and allow to dry without wiping.
Children under 6 years of age should be supervised when using this product.
Other Information
do not store above 104F (40C)
may discolor certain fa surfaces.
Inactive Ingredient
WATER,PHENOXYETHANOL,CARBOMER COPOLYMER TYPE A,SODIUM HYDRIDE,DMDM HYDANTOIN ,FD&C BLUE NO. 1,FD&C YELLOW NO. 5
Package Label.Principal Display Panel
Phot Of Druglisting (3)
Image Description (4)
Image Description (5)
Image Description (1)
Image Description (2)
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