Active Ingredient(S)
Ethyl alcohol 75% v/v. Purpose: Antiseptic
Hand Sanitizer
FDA Label NDC 76390-0101
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Shanghai Soap Co., Ltd. for the product Hand Sanitizer (NDC 76390-0101). 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, otc - 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
Antiseptic
Use
Hand sanitizer to help reduce bacteria.
Warnings
For external use only.
Flammable. Keep away from heat or flame.
Otc - Do Not Use
Do not use in or near the eyes.
Otc - When Using
When using this product do not use in or near the eyes.
If case of contact, rinse eyes thoroughly with water.
Otc - Stop Use
Stop use and ask a doctor if irritation or rash occurs.
Thess may be signs of a serious condition.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center.
Directions
Place enough product on hands to cover all surfaces.
Other Information
Store between 15-30℃ (59-86℉).
Inactive Ingredients
Water (Aqua), Acrylates/C10-30 Alkyl/Acrylate Crosspolymer, Triethanolamine, Glycerin, Aloe Extract, Panthenol (pro-Vitamin B5)
Package Label - Principal Display Panel
060 (060)
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