Active Ingredient
Ethanol 75% (V/V)
Baby Beluga Instant Hand Sanitizer
FDA Label NDC 79425-500
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Zhongshan Tentop Fine Chemical Co., Ltd. for the product Baby Beluga Instant Hand Sanitizer (NDC 79425-500). 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, do not use, when using this product, stop use and ask a doctor, 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
Uses
To reduce bacteria on hand
Warnings
For external use only.
Flammable, keep away from heat or flame.
Do Not Use
- in children less than 2 months of age
- on open skin wounds
When Using This Product
When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop Use And Ask A Doctor
Stop use and ask a doctor if irritation or rash occurs.
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
- Place enough amount of product on hands to cover all surface. Rub hands until dry.
- Supervise children under 6 years old when using this product to avoid swallowing.
Other Information
- Store between 15-30°C (59-86°F).
- Avoid freezing and excessive heat above 40°C (104°F).
Inactive Ingredients
Acrylates/c10-30 alkyl acrylate crosspolymer, Glycerin, Tocopherol, Triethanolamine, Water.
Package Label/Principal Display Panel
NDC 79425-500-01; 500 ml
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