FDA.reportPublic FDA data

Guy Laroche Paris Drakkar Essence Antiperspirant Deodorant

Manufacturer
L'Oreal USA Products Inc | Les Emballages Facoteck Inc,
Effective date
2022-01-04
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 22:19:11

Label at a glance#

ProductGuy Laroche Paris Drakkar Essence Antiperspirant Deodorant
Active ingredientAluminum zirconium tetrachlorohydrex gly
Label structure11 sections

Dosage and administration

apply to underarms only

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum zirconium tetrachlorohydrex gly 16%

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

isopropyl palmitate, dimethicone, stearyl alcohol, hydrogenated castor oil, aluminum starch octenylsuccinate, PEG-8 distearate, PPG-14 butyl ether, fragrance, nylon-12, synthetic wax, water, disteardimonium hectorite, calcium hydroxide, limonene, linalool, benzyl salicylate, benzyl alcohol, hydroxycitronellal, hexyl cinnamal, coumarin, geraniol, alpha-isomethyl ionone, citronellol, citral

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of a labelimage of a label

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
Aluminum zirconium tetrachlorohydrex glyACTIVE INGREDIENT8O386558JE1
ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLYACTIVE MOIETY8O386558JE1

Products#

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

DailyMed product names page 1 of 1 · 25 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49967-93749967-937-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 24 matching rows.

Name, UNII, Kind table
NameUNIIKind
Aluminum zirconium tetrachlorohydrex gly8O386558JEACTIB
ISOPROPYL PALMITATE8CRQ2TH63MIACT
DIMETHICONE92RU3N3Y1OIACT
STEARYL ALCOHOL2KR89I4H1YIACT
HYDROGENATED CASTOR OILZF94AP8MEYIACT
ALUMINUM STARCH OCTENYLSUCCINATEI9PJ0O6294IACT
PEG-8 DISTEARATE7JNC8VN07MIACT
PPG-14 BUTYL ETHERR199TJT95TIACT
NYLON-12446U8J075BIACT
SYNTHETIC WAX (1200 MW)Q3Z4BCH099IACT
WATER059QF0KO0RIACT
DISTEARDIMONIUM HECTORITEX687XDK09LIACT
CALCIUM HYDROXIDEPF5DZW74VNIACT
LIMONENE, (+)-GFD7C86Q1WIACT
LINALOOL, (+/-)-D81QY6I88EIACT
BENZYL SALICYLATEWAO5MNK9TUIACT
BENZYL ALCOHOLLKG8494WBHIACT
HYDROXYCITRONELLAL8SQ0VA4YURIACT
.ALPHA.-HEXYLCINNAMALDEHYDE7X6O37OK2IIACT
COUMARINA4VZ22K1WTIACT
GERANIOLL837108USYIACT
ISOMETHYL-.ALPHA.-IONONE9XP4LC555BIACT
.BETA.-CITRONELLOL, (R)-P01OUT964KIACT
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
7dd8784e-7d54-4562-924f-dd3e4627d44034c30f6c-1983-4221-94de-deee14d512c02022-01-04WarningsExact identifier
spl id: 7dd8784e-7d54-4562-924f-dd3e4627d440
spl set id: 34c30f6c-1983-4221-94de-deee14d512c0

Reported adverse events (FAERS/openFDA)#

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