Active Ingredient(S)
Alcohol 66% v/v. Purpose: Antiseptic
Babingtonsoapco
FDA Label NDC 80104-111
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Babington Soap Co Limited for the product Babingtonsoapco (NDC 80104-111). 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 - when using, otc - stop use, otc - keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic, Hand Sanitizer
Use
Hand Sanitizer to help reduce bacteria on the skin.
Warnings
Flammable. Keep away from fire or flame
For external use only.
Otc - When Using
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 if irritation and redness develop.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Otc - Stop Use
Stop use and ask a doctor if irritation and redness develop.
Otc - 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
- Dispense onto dry hands and rub together thoroughly and then allow product to dry without rinsing. Do not use on open skin or wounds.
- Not for use by children under 6 years old.
Other Information
- Do not store above 106F.
- If skin irritation or rash occurs discontinue use immediately.
- May discolor some fabrics.
Inactive Ingredients
Aqua, Polyquaternium 10, Chitosan, lactic acid organic, lemongrass oil.
Package Label - Principal Display Panel
55 mL NDC: 80104-111-11
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