FDA.reportPublic FDA data

Kiehls CrossTerrain Antiperspirant Deodorant

Manufacturer
KDC/ONE Development Corporation, Inc | L'Oreal USA Products Inc | Summit Research Labs, Inc
Effective date
2021-09-01
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
legacy-cache
Hydrated at
2026-08-01 22:37:01

Label at a glance#

ProductKiehls CrossTerrain Antiperspirant Deodorant 24 Hour Strong Dry
Active ingredientALUMINUM CHLOROHYDRATE
Label structure10 sections

Indications and uses

Use reduces underarm wetness

Dosage and administration

Use reduces underarm wetness

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum Chlorohydrate 20%

Inactive Ingredients

INACTIVE INGREDIENT SECTION

cyclopentasiloxane, mineral oil, stearyl alcohol, hydrogenated castor oil, cetyl alcohol, talc, PEG-100 stearate, glyceryl stearate, fragrance, limonene, lirnalol, benzyl alcohol, citronellol, benzyl salicylate, geraniol, coumarin, citral

Uses Directions

OTC - PURPOSE SECTION

Use reduces underarm wetness

WARNINGS SECTION

Warnings

For external use only

Uses

INDICATIONS & USAGE SECTION

For underarms only

DOSAGE & ADMINISTRATION SECTION

Directions apply to underarms only.

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have kidney disease.

OTC - DO NOT USE SECTION

DO NOT USE on broken skin

KEEP OUT OF REACH OF CHILDREN

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.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of labelimage of label

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
54565-390154565-3901-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
TALC7SEV7J4R1UIACT
PEG-100 STEARATEYD01N1999RIACT
ALUMINUM CHLOROHYDRATEHPN8MZW13MACTIB
GLYCERYL STEARATE CITRATEWH8T92A065IACT
CYCLOMETHICONENMQ347994ZIACT
STEARYL ALCOHOL2KR89I4H1YIACT
CETYL ALCOHOL936JST6JCNIACT
HYDROGENATED CASTOR OILZF94AP8MEYIACT
MINERAL OILT5L8T28FGPIACT

Source Document#

Source XML · Source PDF

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
caf2318f-b311-74c6-e053-2a95a90a315d5cdd057d-0434-10ce-e053-2991aa0af3fa2021-09-01WarningsExact identifier
spl id: caf2318f-b311-74c6-e053-2a95a90a315d
spl set id: 5cdd057d-0434-10ce-e053-2991aa0af3fa

Reported adverse events (FAERS/openFDA)#

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