Active Ingredient
Aluminum Chlorohydrate 16.0%
Dial Professional Roll On Anti Perspirant Deodorant Solution
FDA Label NDC 54340-018
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Henkel Corporation for the product Dial Professional Roll On Anti Perspirant Deodorant (NDC 54340-018). 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, when using this product, stop using and ask doctor if, 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
Antiperspirant
Uses
Reduces underarm wetness
Warnings
Warnings
For external use only
Do not use on broken skin
Stop use if rash or irritation occurs
Ask a doctor before use if you have
kidney disease.
Keep out of reach of children. If
swallowed, get medical help or contact
a Poison Control Center right away
When Using This Product
- avoid contact with eyes. In case of eye contact, flush with water.
Stop Using And Ask Doctor If
- irritation or redness develops
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact Poison Control Center right away.
Directions
apply to underarms only
Inactive Ingredients
Inactive Ingredients:
Aqua (Water, Eau) · Steareth-2 ·
Steareth-21 . Phenoxyethanol .
Parfum (Fragrance) . PPG-15
Stearyl Ether . Aluminum Starch
Octenylsuccinate
Questions?
1-877-777-3277
Package Label.Principal Display Panel
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