Active Ingredient
ALCHOL 70%
Alcomax
FDA Label NDC 75700-301
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Conic Co., Ltd. for the product Alcomax (NDC 75700-301). 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, inactive ingredient, direction, do not use, when using this product, warnings, 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
ANTIMICROBIAL
Inactive Ingredient
Water, Aloe Barbadensis leaf, chamaecyparis Obtusa leaf, Glycerin, Carbomer, Arqinine, DISODIUM EDTA
Direction
Place enough product on hands to cover all surfaces.Rub hands together until dry.
Supervise children under 6 years of age when using this product to avoid swallowing.
Do Not Use
In children less than 2 months of age .
On open skin wounds
When Using This Product
Keep out of eyes, ears, and mouth in case of contact with eyes, rinse eyes thoroughly whit water.
Warnings
for external sue only. Flammable. keep away from heat or flame
Keep Out Of Reach Of Children.
If swallowed get medical help or contact a Poison Control center right away.
Stop Use And Ask A Doctor.
if irritationor rash occurs. These may be signs of a serious contion.
Use
Hand sanitizer to help reduce bacteria that potentially can cause disease.
For use when soap and water are not avaliable.
Other Information
Store between 33.8~86'F
Avoid freezing and excessive heat
Pakage Label
500ml Ndc:75700-301-01 Label (Label)
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