Active Ingredient(S)
Ethyl Alcohol 70% v/v
Hand Sanitizer Gel
FDA Label NDC 41366-054
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Zhejiang Meimi Technology Co., Ltd. for the product Hand Sanitizer (NDC 41366-054). 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, 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
Purpose
Antimicrobial
Use
Uses hand sanitizer to help reduce bacteria on skin.
Warnings
- For external use only.
- Flammable. Keep away from heat or flame.
Do Not Use
Do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.
Otc - Stop Use
Stop use and ask a doctor if irritation, excessive redness or rash develops.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. Supervise children under 6 years of age when using this product to avoid swallowing. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Put a dime sized drop onto hands and rub together briskly until dry.
Other Information
Store below 110℉(43℃).
Inactive Ingredients
Water, glycerin, propylene glycol, fragrance, carbomer, triethanolamine, blue 1, yellow 5.
Package Label - Principal Display Panel
59 mL in 1 BOTTLE
NDC: 41366-054-01
59ml Label (59ml 7)
* Please review the disclaimer below.
