Active Ingredient
Ethyl alcohol 70%
Ollie Hand Sanitizer
FDA Label NDC 81634-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by F.p. Aromatics Singapore Pte Ltd for the product Ollie Hand Sanitizer (NDC 81634-001). 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, purpose, uses, warnings, direction, other information, inactive ingredient, product label, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Uses
To sanitize hand when soap and water are not available.
Warnings
For external use only. Keep away from fire or flame.
Do not use
- on open wounds
- on children less than 4 months of age.
When using this product, keep out of eyes, ears, mouth.
Stop use and ask a doctor if irritation or rash occurs.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away
Direction
- Spray on hands and rub them together gently
- Supervise children under 6 years of age in the use of this product
Other Information
Store between 15° - 30°C (59° - 86°F)
Inactive Ingredient
Aloe vera, Orange oil, Peppermint oil, Tea tree oil, Water
Product Label
Image Description (Image V2)
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