Otc - Active Ingredient
Active Ingredients Aluminum Chlorohydrates 20%
Ultra Dry Antiperspirant
FDA Label NDC 29500-9211
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Personal Care Products for the product Ultra Dry Antiperspirant (NDC 29500-9211). 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 otc - active ingredient, otc - purpose, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, inactive ingredient, 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
Otc - Purpose
Purpose Antiperspirant
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, seek medical help or contact a Poison Control Center immediately.
Indications & Usage
Uses reduces underarm wetness and perspiration.
Warnings
Warnings
For external use only
Stop use and ask a doctor if irritation or rash develops.
Dosage & Administration
Directions
Remove cap, turn dial to raise product, apply evenly to underarms only, replace cap after use.
Inactive Ingredient
Inactive Ingredients mineral oil, stearic acid, stearyl alcohol, talc, octyl palmitate, cyclopentasiloxane, hydrogenated, castor oil, fragrance, PPF-14 butyl ehter, PEG-8 distearate, BHT.
Package Label.Principal Display Panel
Compare to Degree Men
anti-perspirant/deodorant
Personal Care
Ultra Dry Anti-perspirant and deodorant
Cool blast Invisible solid
Net wt. 2 oz (57 g)
Pc Coolblastdeo Label (Pc Coolblastdeo)
* Please review the disclaimer below.
