Talon Antiseptic Wipes
FDA Label NDC 79891-003
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Dobolv (quanzhou) Paper Co., Ltd for the product Talon Antiseptic Wipes (NDC 79891-003). 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 drug facts, active ingredients, purpose, uses, warnings, 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
Active Ingredients
Alcohol 70% (V/V)
Benzalkonium Chloride 0.10% (W/V)
Purpose
Antiseptic
Uses
• for hand washing to decrease bacteria on the skin.
• Recommended for repeat use.
Warnings
For external use only. Flammable.
Keep away from heat or flame.
Do not use if you have been diagnosed by a physician as being allergic to any of the ingredients.
When using this product Keep out of eyes. If contact occurs, rinse thoroughly with water.
Stop use and ask a doctor if irritation or redness develops, and if condition persists for more than 71 hours.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children unless under adult supervision, If swallowed seek medical assistance.
Directions
• Wet hands thoroughly with product and allow to dry without rinse.
• Children under six years of age should be supervised when using this product.
Other Information
• Store in a dry place away from fire.
• Manufacturing/Expiry Date: See package for details
Inactive Ingredients
Aloe Vera Extract, Betaine, Citric acid, Dodecyl polyglucoside, Glycerol, Hexadecylpyridinium Chloride, Propanediol, Sodium citrate, Vitamin E, Water(Aqua).
Packaging
Image (7989100310)
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