Active Ingredient
Aluminum Zirconium Octachlorohydrex GLY 16.4%
Soft And Dri Dri Gel
FDA Label NDC 51815-217
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 for the product Soft And Dri Dri Gel (NDC 51815-217). 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, warnings, keep out of reach of children., otc - ask doctor, use, inactive ingredients, otc - questions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiperspirant
Warnings
For external use only
Do not use on broken skin
Stop use and ask a doctor if rash or irritation occurs
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact poison control center right away
Otc - Ask Doctor
Ask doctor before use if you have kidney disease
Use
Reduces underarm perspiration
Inactive Ingredients
Water, alcohol
denat., cyclomethicone, propylene glycol,
dimethicone, trisiloxane, calcium chloride,
PEG/PPG-18/18 dimethicone, fragrance
Otc - Questions
For questions or the latest product news,
visit www.softndri.com
Directions
Apply to underarms only
Package Label.Principal Display Panel
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