Active Ingredient
Ethyl Alcohol 62%
Hand Sanitizer (rinse-free)
FDA Label NDC 75129-001
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 Rayshine Envi-tech Developing Co., Ltd. for the product Hand Sanitizer (rinse-free) (NDC 75129-001). 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, uses, warnings, when using this product, directions, inactive ingredients, package label - principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Uses
For hand sanitizing to reduce bacteria
on the skin.
Warnings
For extermal use only-hands. Flamable.Keep awaysfrom fire and flame.
When Using This Product
Keep out of eyes.Do not inhale or ingest. Stop use and ask a doctor if skinimitation develops. Keep out of reach of children.
Directions
Squeez small amount in your palm and briskly rub hands together until dry.
Inactive Ingredients
Water,Carbomer,Triethanolamine,Glycerin,Vitamin E,Aloe Barbadensis.Fragrance.
Package Label - Principal Display Panel
30 mL Label (Label1)
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