Active Ingredient(S)
Ethanol Alcohol 62% w/v. Purpose: Antiseptic
Advanced Gel Hand Sanitizer Soothing Lavender
FDA Label NDC 81209-200
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Bluetrack Inc for the product Advanced Gel Hand Sanitizer Soothing Lavender (NDC 81209-200). 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, otc - when using, directions, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic, Advanced Hand Sanitizer Soothing Lavender
Use
For Sanitizing hands to reduce bacteria and virus on the skin
Warnings
Flammable. Keep away from fire or flame
For external use only.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children or pets.
Otc - When Using
Do not put in eyes
Directions
Apply Small amount in your palm and briskly rub hands together until dry.
Inactive Ingredients
Inactive Ingredients:Water, Glycerin, Carbomer, Fragrance, Aloe Barbadensis Leaf Juice, Aminomethyl Propanol, Vitamin E, Iron Oxide(CI 77499),Iron Oxide(CI 77492), D&C Red No.30.
Package Label - Principal Display Panel
5000 mL NDC: 81209-200-01
1000mL NDC: 81209-200-02
5000ml (Bluetrack Sanitizer Fda 5l Lavender Label)
1000ml (Bluetrack Sanitizer Fda 1l Lavender Label)
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