Active Ingredients
Ethyl Alcohol 70%
Hand Sanitizer
FDA Label NDC 69912-009
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Nanomateriales, S.a. De C.v. for the product Hand Sanitizer (NDC 69912-009). 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 ingredients, otc - purpose, use, warnings, do not use, 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
Otc - Purpose
Purpose: Antiseptic
Use
For hand washing to decrease bacteria on the skin.
Warnings
For external use only. Flammable. Keep away from heat or flame
Do Not Use
- in the eyes
Otc - Stop Use
Stop use and ask a doctor if irritation and redness develop. Condition persists for more than 72 hours.
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
- Wet hands thoroughly with product and allow to dry without wiping
Other Information
- Store between 59-86°F (15-30°C)
- Avoid freezing and excessive heat above (40°C) 104°F
Inactive Ingredients
Carbomer, glycerin, fragrance, triethanolamine, water, zinc oxide, zinc pyrithione
Package Label.Principal Display Panel
200000 mL NDC 69912-009-06
200l (200l)
60 mL NDC 69912-009-05
60ml (60ml)
500 mL NDC 69912-009-03
500ml (500ml)
250 mL NDC 69912-009-04
250ml (250ml)
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