Otc - Active Ingredient
Alcohol
Chopima Hand Sanitizer
FDA Label NDC 69969-601
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Soriso for the product Chopima Hand Sanitizer (NDC 69969-601). 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 package label.principal display panel, otc - active ingredient, dosage & administration, otc - purpose, indications & usage, inactive ingredient, otc - keep out of reach of children, warnings, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Dosage & Administration
For external only
Otc - Purpose
Antiseptic
Indications & Usage
Apply to clean, dry hands. Apply sufficient amount to thoroughly wet all surfaces of hands and fingers. Rub onto hands until dry.
Supervise children in the use of this product.
Inactive Ingredient
Water
Glycerin
Fragrance
Carbomer
Triethanolamine
Butylene Glycol
Mulberry Root Extract
Aloe Extract
Allantoin
Otc - Keep Out Of Reach Of Children
KEEP OUT OF REACH OF CHILDREN
Warnings
For external use only.
Flammable. Keep away from fire or flame.
Do not use in eyes.
If swallowed, get medical help promptly.
Stop use, ask doctor if irritation occurs.
Keep out of reach of children.
* Please review the disclaimer below.
