Otc - Active Ingredient
Active ingredients
Ethyl alcohol 65%
Hand Sanitizer
FDA Label NDC 47993-279
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Ningbo Jiangbei Ocean Star Trading Co.,ltd for the product Hand Sanitizer (NDC 47993-279). 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 otc - active ingredient, otc - purpose, indications & usage, warnings, otc - do not use, otc - stop use, otc - keep out of reach of children, dosage & administration, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Antiseptic
Indications & Usage
Uses：
For hand washing to decrease bacteria on th skin.
Warnings
Warnings:
For external use only.
Flammable，Keep away from heat or flame.
Otc - Do Not Use
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.
Dosage & Administration
Directions:
Wet hands thoroughly with product and allow to dry without wiping.
Other Safety Information
Other information
- Do not store above 104℉(40℃)
- May discolor some fabrics or surfaces
Inactive Ingredient
Inactive Ingredients:
Water,glycerol,aloe vera leaf juice,carbomer,triethanolamine.
Package Label.Principal Display Panel
1000ml (1000ml)
500ml (500ml)
60ml (60ml)
30ml (30ml)
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