Active Ingredient
Triclocarban 0.30%
Dial Aloe
FDA Label NDC 51815-302
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Vvf Illinois Services Llc for the product Dial Aloe (NDC 51815-302). 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, keep out of reach of children, use, warnings, inactive ingredients, questions, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
ANTIBACTERIAL
Keep Out Of Reach Of Children
If swallowed, get medical
help or contact Poison Control right away.
Use
For washing to decrease bacteria on the skin
Warnings
For external use only
When using this product
Avoid contact with eyes. In case of eye contact, flush with water
Stop using and ask doctor if irritation and redness develops
Inactive Ingredients
SOAP, (SODIUM COCOATE*, SODIUM PALM KERNELATE*, SODIUM PALMATE*, SODIUM TALLOWATE*), WATER, TALC, COCONUT ACID*, PALM ACID*, TALLOW ACID, PALM KERNEL ACID*, PEG-G METHYL ETHER, FRAGRANCE, SUNFLOWERSEEDAMIDOPROPYL ETHYLDIMONIUM ETHOSULFATE, PEG-9, GLYCERIN, SORBITOL, SODIUM CHLORIDE, ALOE BARBADENSIS LEAF JUICE, PENTASODIUM PENTETATE, TETRASODIUM ETIDRONATE, TITANIUM DIOXIDE, YELLOW 5, GREEN 3.
Questions
1-800-258- DIAL (3425)
Package Label.Principal Display Panel
Aloe.jpg (Aloe)
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