FDA.reportPublic FDA data

Kiehls Since 1851 CrossTerrain Antiperspirant Deodorant 24 hour Strong Dry

Manufacturer
L'Oreal USA Products Inc | Les Emballages Facoteck Inc.
Effective date
2022-01-04
Label type
HUMAN OTC DRUG LABEL
Version
13
Source
legacy-cache
Hydrated at
2026-08-01 22:19:18

Label at a glance#

ProductKiehls Since 1851 CrossTerrain Antiperspirant Deodorant 24 hour Strong Dry
Active ingredientALUMINUM CHLOROHYDRATE
Label structure11 sections

Dosage and administration

apply to underarms only

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum chlorohydrate 20%

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Use

INDICATIONS & USAGE SECTION

reduces underarm wetness

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

on broken skin

Stop use if

OTC - STOP USE SECTION

rash or irritation occurs

Ask a doctor before use if

OTC - ASK DOCTOR SECTION

you have kidney disease

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

apply to underarms only

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of a labelimage of a label

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
Aluminum ChlorohydrateACTIVE INGREDIENTHPN8MZW13M10
Aluminum CationACTIVE MOIETY3XHB1D032B10

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49967-27249967-272-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALUMINUM CHLOROHYDRATEHPN8MZW13MACTIB
CYCLOMETHICONE 50THT5PCI0RIACT
MINERAL OILT5L8T28FGPIACT
STEARYL ALCOHOL2KR89I4H1YIACT
HYDROGENATED CASTOR OILZF94AP8MEYIACT
CETYL ALCOHOL936JST6JCNIACT
TALC7SEV7J4R1UIACT
PEG-100 STEARATEYD01N1999RIACT
LIMONENE, (+)-GFD7C86Q1WIACT
LINALOOL, (+/-)-D81QY6I88EIACT
BENZYL ALCOHOLLKG8494WBHIACT
.BETA.-CITRONELLOL, (R)-P01OUT964KIACT
BENZYL SALICYLATEWAO5MNK9TUIACT
GERANIOLL837108USYIACT
COUMARINA4VZ22K1WTIACT
CITRALT7EU0O9VPPIACT

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
bb9fd263-42f4-487d-9640-f5d4c461382f9b01bafd-edda-4e0f-9d68-e684ba7de42b2023-01-26WarningsExact identifier
spl set id: 9b01bafd-edda-4e0f-9d68-e684ba7de42b

Reported adverse events (FAERS/openFDA)#

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