Active Ingredient(S)
0.3% Benzalkonium chloride
Hand Sanitizer
FDA Label NDC 14341-006
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Ningbo Venus Cosmetic Co., Ltd. for the product Hand Sanitizer (NDC 14341-006). 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(s), purpose, directions, warnings, do not use, otc - when using, otc - stop use, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Use when needed.
Directions
Spray hand sanitizer in the palm of your hands.
Rub briskly product onto hands and allow to dry.
Spray hand sanitizer in the palm of your hands.
Rub briskly product onto hands and allow to dry.
Warnings
For external use only. Avoid contact with eyes. If contact occurs, flush eyes with water. If the condition persists, consult a doctor.
If swallowed immediately call a poison control center or a doctor for treatment advice.
Do Not Use
/
Otc - When Using
For external use only. Avoid contact with eyes. If contact occurs, flush eyes with water. If the condition persists, consult a doctor.
Otc - Stop Use
If swallowed immediately call a poison control center or a doctor for treatment advice.
Other Information
Store at temperatures below 30°C.
Inactive Ingredients
Water, Glycerine, Decyl Glucoside, Aloe Vera, Fructooligosaccharide, Fragrance
Package Label - Principal Display Panel
250 (250)
400 (400)
50 (50)
100 (100)
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