Active Ingredient
Aluminum Zirconium Pentachlorohydrex GLY 18% (Anhydrous)
Exchange Select Powder Fresh Deodorant Stick
FDA Label NDC 85161-222
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Longway Technology(guangzhou)co., Ltd. for the product Exchange Select Powder Fresh Deodorant (NDC 85161-222). 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, use, warnings, do not use, ask a doctor, stop use if, keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiperspirant
Use
reduces underarm wetness
Warnings
For external use only
Do Not Use
on broken skin
Ask A Doctor
before use if you have kidney disease
Stop Use If
rash or irritation occurs
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center immediately.
Directions
Apply to underarms only
Inactive Ingredients
Cyclopentasiloxane, Dimethicone, Mineral Oil, Petrolatum, Stearyl Alcohol, Hydrogenated Castor Oil, Fragrance, PPG-14 Butyl Ether, Behenyl Alcohol, BHT
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