Active Ingredient(S)
alcohol
Bonange Dr,plus Sanitizer
FDA Label NDC 78761-0002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Bonange Korea Inc for the product Bonange Dr, Plus Sanitizer (NDC 78761-0002). 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 - keep out of reach of children, directions, inactive ingredient, 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
Purpose: Antiseptic
Use
Hand sanitizing to help reduce bacteria on the skin
Warnings
For external use only.
when using this product, avoid contact with the eyes. In case of contact, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or redness appears and lasts.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.
Directions
• Place enough product on hands to cover all surfaces. Rub hands together until dry.
• Supervise children under 6 years of age when using this product to avoid swallowing.
Inactive Ingredient
Water
Glycern
Phenoxyethanol
Cabomer
Triethanolamine
Butylene Glycol
1,2-Hexanediol
OpuntiaFicus-Indica Extract
Bambusa Vulgaris Leaf/Stem Extact
AvenaSativa(oat)kemel Ext
Luffa Cylindrica Fruit Ext
Aloe Barbadensis Leaf Ext
Salvia Hispanica Seed Ext
Cocos Nucifera(Coconut)Fruit
ButyrospermumParkil(Shea)Butter Ext
scutellariaBaicalensis Ext
LaminariaJaponica Ext
Ethylhexylglycerin
Package Label.Principal Display Panel
Label (Label)
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