FDA.reportPublic FDA data

Jafra Daily Antiperspirant Deodorant Roll-on

Manufacturer
Distribuidora Comercial Jafra, S.A. de C.V. | Jafra Cosmetics International
Effective date
2025-01-02
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 00:50:34

Label at a glance#

ProductJafra Daily Antiperspirant Deodorant Roll-on
Active ingredientALUMINUM CHLOROHYDRATE
Label structure9 sections

Indications and uses

Reduces underarm wetness

Dosage and administration

apply to underarms only

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Aluminum Chlorohydrate 12.3% 

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Uses

INDICATIONS & USAGE SECTION

Reduces underarm wetness

Warnings

WARNINGS SECTION

For external use only
Do not use on broken skin
Stop use if rash or irritation occurs
Ask a doctor before use if you have kidney disease

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

apply to underarms only

INACTIVE INGREDIENT SECTION

Inactive Ingredients


Water, PEG-40 Stearate, PEG-25 Propylene Glycol Stearate, Stearic Acid, Sorbitan Sesquioleate, Cetyl Alcohol, Magnesium Aluminum Silicate, Fragrance/Parfum, DMDM Hydantoin, Iodopropynyl Butylcarbamate, Amyl Cinnamal, Benzyl Alcohol, Eugenol, Hydroxycitronellal, Benzyl Salicylate, Coumarin, Butylphenyl Methylpropional, Linalool, Benzyl Benzoate, Citronellol, Limonene, Alpha-Isomethyl Ionone

SPL UNCLASSIFIED SECTION

Questions?


Call 1-800-551-2345 or visit www.jafra.com

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68828-702-01Jafra Daily Antiperspirant Deodorant Roll-on60 mL in 1 BOTTLE, WITH APPLICATORLIQUID604
68828-702-02Jafra Daily Antiperspirant Deodorant Roll-on1 in 1 CARTONLIQUID14

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68828-702JAFRA DAILY ANTIPERSPIRANT DEODORANT ROLL-ON (ALUMINUM CHLOROHYDRATE) LIQUID [DISTRIBUIDORA COMERCIAL JAFRA, S.A. DE C.V.]4Current NDC, Legacy NDC, 2 package rows20250104_4e7a8a3b-12de-4108-a11c-4838510934a5.zip

Products#

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

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
68828-70268828-702-01, 68828-702-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 22 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
PEG-40 MONOSTEARATEECU18C66Q7IACT
PEG-25 PROPYLENE GLYCOL STEARATEX21KPH4633IACT
STEARIC ACID4ELV7Z65APIACT
SORBITAN SESQUIOLEATE0W8RRI5W5AIACT
MAGNESIUM ALUMINUM SILICATE6M3P64V0NCIACT
DMDM HYDANTOINBYR0546TOWIACT
IODOPROPYNYL BUTYLCARBAMATE603P14DHEBIACT
CETYL ALCOHOL936JST6JCNIACT
.ALPHA.-AMYLCINNAMALDEHYDEWC51CA3418IACT
BENZYL ALCOHOLLKG8494WBHIACT
EUGENOL3T8H1794QWIACT
HYDROXYCITRONELLAL8SQ0VA4YURIACT
BENZYL SALICYLATEWAO5MNK9TUIACT
COUMARINA4VZ22K1WTIACT
BUTYLPHENYL METHYLPROPIONALT7540GJV69IACT
LINALOOL, (+/-)-D81QY6I88EIACT
BENZYL BENZOATEN863NB338GIACT
.BETA.-CITRONELLOL, (R)-P01OUT964KIACT
LIMONENE, (+)-GFD7C86Q1WIACT
ISOMETHYL-.ALPHA.-IONONE9XP4LC555BIACT
ALUMINUM CHLOROHYDRATEHPN8MZW13MACTIB

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
Jafra Daily Antiperspirant Deodorant Roll-onALUMINUM CHLOROHYDRATEDistribuidora Comercial Jafra, S.A. de C.V.4e7a8a3b-12de-4108-a11c-4838510934a52025-01-02WarningsExact identifier
ndc (package): 68828-702-02
ndc (package): 68828-702-01
ndc (product): 68828-702
ndc11 (package): 68828070202
ndc11 (package): 68828070201
spl id: 2abe0121-d9af-92c1-e063-6294a90afa54
spl set id: 4e7a8a3b-12de-4108-a11c-4838510934a5

Reported adverse events (FAERS/openFDA)#

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