Active Ingredient(S)
Alcohol 65% v/v. Purpose: Antimicrobial
Hand Sanitizer
FDA Label NDC 69980-101
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Shandong Vianor Healthy Science Co., Ltd. for the product Hand Sanitizer (NDC 69980-101). 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, use, warnings, do not use, otc - when using, otc - stop use, otc - 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
Use
Hand sanitizer to help reduce bacteria on the skin.
Warnings
Flammable. Keep product away from open flames.
For external use only.
Do Not Use
Do not use on children less than 2 months of age.
Do not use on open skin wounds.
Otc - When Using
When using this product, avoid contact with eyes and broken skin.
In case of contact with eyes, rinse immediately with water.
Otc - Stop Use
If skin irritation occurs, discontinue use. Consult a doctor if rash persit.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children and superise during use.
Directions
Rua hands throughly with gel and let dry.
Other Information
Do not strore above 110℉/43℃.
Inactive Ingredients
Water, VE.
Package Label - Principal Display Panel
60 (60)
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