Active Ingredient
Aluminum Zirconium Octachlorohydrex Gly (16.4%)
Soft And Dri Drigel
FDA Label NDC 69752-102
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by The Village Company for the product Soft And Dri Drigel (NDC 69752-102). 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, otc - purpose, use, warnings for external use only, stop use and ask a doctor if, keep out of reach of chlidren, ask a doctor before use if, do not use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Antiperspirant
Use
reduces underarm perspiration
Warnings For External Use Only
Stop Use And Ask A Doctor If
rash or irritation occurs
Keep Out Of Reach Of Chlidren
If swallowed, get medical help or contact a posion control center right away
Ask A Doctor Before Use If
you have kidney disease
Do Not Use
on broken skin
Directions
Apply to underarms only.
Dosage & Administration
Apply to underarms only.
Inactive Ingredients
Water, ( Auqua, EAU), Alcohol denat., Cyclopentsiloxane, Propylene Glycol, Dimethicone, Calcium cholride, Trisiloxane, Pentasiloxane, PEG/PPG-18/18, Dimethicone, T-butyl alcohol, Denaton-ium Benzoate, Fragrance (Parfum), Benzyl Salicylate, Cirtronellol, Benzyl Alcohol, Geraniol, Limonene
Package Label.Principal Display Panel
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