Active Ingredient(S)
Benzalkonium Chloride 0.13%. Purpose: Antiseptic
San Skinlab Cloth Wet Wipes Cloth
FDA Label NDC 75214-120
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Hanul Co.,ltd for the product San Skinlab Cloth Wet Wipes (NDC 75214-120). 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 - when using, 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
Antiseptic,
Use
to decrease bacteria on the skin that could cause disease
Warnings
For external use only.
Otc - When Using
Keep out of eyes, in case of contact with eyes, flush thoroughly with water, Avoid contact with broken skin, Do Not inhale or ingest
Otc - Stop Use
Stop use and ask a doctor if irritation or redness developes condition persist 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
Not recommended for infants
Other Information
- Do not Store above 105F/40 Degree .Do not Freeze
- Dispose of used wipe in trash, do not flush into toilet
Inactive Ingredients
Water ( Aqua) , Alcohol ( Ethanol). Glycerin,Butylene Glycol, Aloe Vera, Citric Acid, 1,2 hexanediol
Package Label - Principal Display Panel
120 Wet wipes NDC 75214-120-01
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