FDA.reportPublic FDA data

Certain Dri Antiperspirant Foot-Lotion

Manufacturer
Clarion Brands, LLC
Effective date
2025-12-23
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:28:18

Label at a glance#

ProductCertain Dri Antiperspirant Foot-Lotion
Active ingredientALUMINUM CHLORIDE
Label structure11 sections

Dosage and administration

wash and dry soles thoroughly before application apply a small, pea sized amount to the soles of your feet rub into soles vigorously for 15 seconds  for best results, apply every night before bed and an additional two times per day for at least four weeks

Label contents#

Full prescribing information#

Active ingredient 

OTC - ACTIVE INGREDIENT SECTION

Aluminum chloride 15%

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

  • on broken or irritated skin
  • immediately after shaving
  • immediately after bathing

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you havekidney disease

OTC - WHEN USING SECTION

When using this productdo not use in or near eyes

OTC - STOP USE SECTION

Stop use and ask a doctor ifrash or irritation develops

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • wash and dry soles thoroughly before application
  • apply a small, pea sized amount to the soles of your feet
  • rub into soles vigorously for 15 seconds 
  • for best results, apply every night before bed and an additional two times per day for at least four weeks

Inactive ingredients

INACTIVE INGREDIENT SECTION

aloe barbadensis leaf juice, artemisia vulgarixs extract, behentrimonium methosulfate, bisaolol, bis-laurl cocaminopropylamine/HDI/PEG-100 copolymer, butylene glycol, cetearyl alcohol, cetyl alcohol, dimethicone, ethylhexyglycerin, hydroxyethylcellulose, jojoba esters, laminaria digitata extract, opuntia ficus-indica fruit extract, potassium hydroxide, saccharomyces cerevisiae extract, water, zingiber officinale (ginger) root extract

Questions? call  1-844-923-7837

PACKAGE LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CERTAIN
DRI ®
ANTIPERSPIRANT

QUICK DRY
SWEAT
GUARD

FOOT
LOTION

CLINICALLY SHOWN
TO REDUCE SWEAT

NET WT 1.3 OZ (36 g)

Distributed by: Certain Dri LLC, 811 Broad Street, Suite 600
Chattanooga, TN 37402 ©2024

1000163

foot lotion label
foot lotion label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69693-726-14Certain Dri Antiperspirant Foot-Lotion1 in 1 CARTONLOTION13
69693-726-14Certain Dri Antiperspirant Foot-Lotion36 mL in 1 TUBELOTION363

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69693-72669693-726-14

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 19 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOE VERA LEAFZY81Z83H0XIACT
ARTEMISIA VULGARIS ROOT32MP823R8SIACT
BEHENTRIMONIUM METHOSULFATE5SHP745C61IACT
LEVOMENOL24WE03BX2TIACT
THIAMINE BIS-LAURYLSULFATE226A8HU328IACT
BUTYLENE GLYCOL3XUS85K0RAIACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
CETYL ALCOHOL936JST6JCNIACT
DIMETHICONE92RU3N3Y1OIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
HYDROXYETHYL CELLULOSE, UNSPECIFIEDT4V6TWG28DIACT
HYDROLYZED JOJOBA ESTERS (ACID FORM)UDR641JW8WIACT
LAMINARIA DIGITATA15E7C67EE8IACT
OPUNTIA FICUS-INDICA FRUIT JUICE5ZC110ZY2HIACT
POTASSIUM HYDROXIDEWZH3C48M4TIACT
SACCHAROMYCES CEREVISIAE978D8U419HIACT
WATER059QF0KO0RIACT
GINGERC5529G5JPQIACT
ALUMINUM CHLORIDE3CYT62D3GAACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Certain Dri Antiperspirant Foot-LotionALUMINUM CHLORIDEClarion Brands, LLC2c2ac262-b37b-4dca-b680-5c89504e2f2c2025-12-23WarningsExact identifier
ndc (package): 69693-726-14
ndc (product): 69693-726
ndc11 (package): 69693072614
spl id: 46a8dbc9-51d4-484d-e063-6394a90a9318
spl set id: 2c2ac262-b37b-4dca-b680-5c89504e2f2c

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.