Foam Hand Sanitizer
- Dosage form
- LIQUID
- Labeler
- Guangdong Kemei Pharmaceutical Technology Co., Ltd.
- Label updated
- 2020-09-19
- Retrieved
- 2026-09-07
- Active ingredients
- SODIUM CHLORIDE
ACTIVE INGREDIENTS
Sodium chloride 1.5%
Purpose
Antiseptic
Uses
Apply proper amount to palm, massage gently until foamy, then rinse with water.
Warnings
This product is for external use only.
When using this product In case of contact with eyes, rinse immediately with plenty of water.
Stop using and ask a doctor if irritation or rash occurs. These may be signs of a serious condition
Flammable. Keep away from heat or flame
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away
Label information
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Label information
When using this product In case of contact with eyes, rinse immediately with plenty of water.
Stop using and ask a doctor if irritation or rash occurs. These may be signs of a serious condition
Flammable. Keep away from heat or flame
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away
Label information
Stop using and ask a doctor if irritation or rash occurs. These may be signs of a serious condition
Flammable. Keep away from heat or flame
Label information
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away
Directions
Scope of application: Household and personal cleaning.
Main Effect Effective inhibition of microorganisms category intestinal bacteria, pyogenic coccus.
Other information
Keep tightly closed. Store between 32°F and 109°F
Inactive ingredients
Citric acid, Cocoamidopropyl betaine, Coconut oil amide DEA, Disodium EDTA, DMDM hydantoin, Essence, Sodium lauryl alcohol polyether sulfate, Water
Package Label - Principal Display Panel
[Image in the official label — see DailyMed source]
[Image in the official label — see DailyMed source]
[Image in the official label — see DailyMed source]
DailyMed Set ID: afa35c57-8ee0-cb47-e053-2995a90a1152 · Version 2
NDC: 75132-012