Active Ingredient(S)
Ethyl Alcohol 75% . Purpose: Antiseptic
Hand Sanitizer
FDA Label NDC 78049-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Guang Dong Meibao Cosmetics Co.,ltd for the product Hand Sanitizer (NDC 78049-001). 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(s), purpose, use, warnings, otc - stop use, otc - keep out of reach of children, directions, other information, 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 for reducing bacteria on the skin that can cause disease.
Warnings
For external use only. Flammable. Keep away from heat or flame
Otc - Stop Use
Stop use and ask a doctor if irritation or or redness appear
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.for children under 6.use only under adult supervision not recommended for infants
Other Information
Do not store above 105℉. may discolor fabric or damage hard surface
Inactive Ingredients
glycerol, water
Package Label - Principal Display Panel
100 mL NDC: 78049-001-01
Package (Package)
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