Home DailyMed 808c4b30-bc0c-4d71-b7ec-118926abcd07 Certain Dri Antiperspirant Hand-Lotion - Clarion Brands, LLC Drug label information. FDA.report displays public Structured Product Labeling data from DailyMed and legacy FDA.report DailyMed cache rows. This page is not medical advice, prescribing advice, or a substitute for the official label reviewed by a qualified healthcare professional. Labeling can change; when a current hydrated DailyMed SPL record is available, FDA.report shows that newer record before legacy cached files.
Manufacturer Clarion Brands, LLC
Effective date 2026-11-09
Label type HUMAN OTC DRUG LABEL
Version 4
Source daily-update
Hydrated at 2026-11-13 02:01:24 Label at a glance# Product Certain Dri Antiperspirant Hand-Lotion
Active ingredient ALUMINUM CHLORIDE
Label structure 13 sections
Dosage and administration wash and dry hands thoroughly before application apply a small, pea sized amount to the palms of your hands rub into palms vigorously for 15 seconds for best results, apply every night before bed and an additional two times per day for at least four weeks
Products# Every source-derived product name is available through these pages.
DailyMed product names page 1 of 1 · 21 matching rows.
Certain Dri Antiperspirant Hand-Lotion Aluminum Chloride ALUMINUM CATION ALOE VERA LEAF ARTEMISIA VULGARIS ROOT BEHENTRIMONIUM METHOSULFATE LEVOMENOL THIAMINE BIS-LAURYLSULFATE BUTYLENE GLYCOL CETOSTEARYL ALCOHOL CETYL ALCOHOL DIMETHICONE ETHYLHEXYLGLYCERIN HYDROXYETHYL CELLULOSE, UNSPECIFIED HYDROLYZED JOJOBA ESTERS (ACID FORM) LAMINARIA DIGITATA OPUNTIA FICUS-INDICA FRUIT JUICE POTASSIUM HYDROXIDE SACCHAROMYCES CEREVISIAE WATER GINGER Ingredients# Every source-derived ingredient row is available through these pages.
DailyMed ingredient rows page 1 of 1 · 19 matching rows.
Older Hydrated Versions# Version, Effective date, Source table Version Effective date Source Hydrated 3 2025-12-23 full-release 2026-06-01 01:28:25
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Matched openFDA labels page 1 of 1 · 1 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.