Active Ingredient
Alcohol 62%
Hand Sanitizer
FDA Label NDC 70939-003
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Dongguang Shuoguo Silicone Products Co., Ltd. for the product Hand Sanitizer (NDC 70939-003). 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, keep out of reach of children, directions, inactive ingredient, 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
Antiseptic
Use
Use for hand-washing to decrease bacteria on
the skin, only when water is not available
Warnings
For etemal use only
Flammabl, keep away from fife and fames
When using this poduct
■do not get intoeyes.
iicnacocur, inine eyes hrougwth water
Stop use and aska doctorif
iritation and redness develop
Keep Out Of Reach Of Children
Keep out of reach of cilden. if sallowed, get
medical help or contact a Poison ControlCenter
right away
Directions
■wethands trougly with poduotd and alw
todry wthout wiping
Inactive Ingredient
Water, PEG-40
Hydrogenated Castor 0il, Fragrance,
AcylatesC10-30 Alkyl Acrylate Crospolymer,
Sodium Hydroxide, Denatonium Benzoate.
Package Label.Principal Display Panel
1 (62)
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