Active Ingredient
Benzalkonium Chloride 0.12%
Dab
FDA Label NDC 72898-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Three Kings Corp for the product Dab (NDC 72898-001). 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, purpose, uses, 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
Uses
- For handwashing to decrease bacteria on the skin
- Recommended for repeated use
Warnings
- For external use only
Otc - When Using
When using this product
- Do not use in or near eyes
Otc - Stop Use
Stop use and ask a doctor if irritation or redness develop.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, seek medical attention or contact Poison Control Center immediately.
Directions
- receive a small amount of foam into palm of hand
- rub thoroughly over all surfaces of both hands
- rub hands together until dry
Other Information
- Store in a cool dry place below 104 F (40 C)
Inactive Ingredients
Water, cocamidopropyl betaine, glycerin, poloxamer 124, phenoxyethanol, benzyl alcohol, dehydroacetic acid, sodium hydroxide, citric acid, D&C Green No. 8
Questions?
Contact Three Kings Corp. at 888-872-2350 Mon-Fri 9 am - 4pm CST
Package Label.Principal Display Panel
dab
HAND PROTECTANT + SANITIZER
MICROBIOLOGICAL DEFENSE SPECTRUM
1.2L (1.26 QT) 40.5 GL OZ
dapprotects.com/healthcare
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