Active Ingredient
Alcohol 75% ±5%
Newrain Hand Sanitizer
FDA Label NDC 56136-312
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Ganzhou Olivee Cosmetic Co., Ltd. for the product Newrain Hand Sanitizer (NDC 56136-312). 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, use(s), warnings, keep out of reach of children., directions, inactive ingredients, packaging, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Use(S)
Hand Sanitizer to help reduce bacteria that can potentially cause disease. For use when soap and water are not available.
Warnings
For external use only.
Flammable. Keep product away from fire or flame.
When using this prouct do not use in or near the eye. In case of contact, rine eyes thoroughly with water.
Stop use and ask a doctor if
irritation or redness develops and persists.
Other Information:
store between 15-30℃ (59-86℉)
avoid freezing and excssive heat above 40℃（104℉）.
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away.
Warning choking Hazard: Small Parts. Not intended for children under 3 years of age.
Directions
Wet hands thoroughly with product and rub hands together until dry.
Inactive Ingredients
Alcohol Denat, Water (Aqua), Glycerin, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol
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