Active Ingredient(S)
Alcohol 75% v/v. Purpose: Antiseptic
Hand Sanitizer
FDA Label NDC 75729-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Ningbo Yaohu Bio-technology Co.ltd for the product Hand Sanitizer (NDC 75729-001). 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(s), purpose, use, warnings, otc - when using, otc - stop use, otc - keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic, Hand Sanitizer
Use
Antiseptic Hand Sanitizer
Warnings
Flammable. Keep away from heat or flame. For external use only.
Otc - When Using
Avoid contact with eyes. In case of contact flush eyes with water.
Otc - Stop Use
Stop use and ask a doctor if redness or irritation develop and persist for more than 72 hours.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Spread on both hands, rub it, let dry.
Inactive Ingredients
Aloe barbadensis gel, carbomer, fragrance, glycerin, propylene glycol, tocopheryl acetate, triethanolamine, water
Package Label - Principal Display Panel
236 mL NDC: 75729-001-01
Pdp (75729 001 01)
500 mL NDC: 75729-001-02
Pdp (75729 001 02)
Pdp (75729 001 03)
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