FDA.reportPublic FDA data

Jafra Daily Sensitive Skin Antiperspirant Deodorant Roll-on

Manufacturer
Distribuidora Comercial Jafra, S.A. de C.V. | Jafra Cosmetics International Inc.
Effective date
2025-01-02
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 00:50:31

Label at a glance#

ProductJafra Daily Sensitive Skin 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 ifrash or irritation occurs
Ask a doctor before use if you havekidney 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, Stearic Acid, PEG-25 Propylene Glycol Stearate, Cetyl Alcohol, Magnesium Aluminum Silicate, Sorbitan Sesquioleate, Phenoxyethanol, Fragrance, Linalool, Ethylhexylglycerin, Limonene, Benzyl Benzoate, Citronellol

SPL UNCLASSIFIED SECTION

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

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage descriptionimage descriptionimage descriptionimage descriptionimage description

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68828-705-01Jafra Daily Sensitive Skin Antiperspirant Deodorant Roll-on60 mL in 1 BOTTLE, WITH APPLICATORLIQUID605
68828-705-02Jafra Daily Sensitive Skin Antiperspirant Deodorant Roll-on1 in 1 CARTONLIQUID15

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68828-705JAFRA DAILY SENSITIVE SKIN ANTIPERSPIRANT DEODORANT ROLL-ON (ALUMINUM CHLOROHYDRATE) LIQUID [DISTRIBUIDORA COMERCIAL JAFRA, S.A. DE C.V.]5Current NDC, Legacy NDC, 2 package rows20250104_0d9b13ff-cd3f-477b-bda4-40e1076584b3.zip

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
68828-70568828-705-01, 68828-705-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
PEG-40 MONOSTEARATEECU18C66Q7IACT
PEG-25 PROPYLENE GLYCOL STEARATEX21KPH4633IACT
SORBITAN SESQUIOLEATE0W8RRI5W5AIACT
CETYL ALCOHOL936JST6JCNIACT
MAGNESIUM ALUMINUM SILICATE6M3P64V0NCIACT
PHENOXYETHANOLHIE492ZZ3TIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
LINALOOL, (+/-)-D81QY6I88EIACT
BENZYL BENZOATEN863NB338GIACT
.BETA.-CITRONELLOL, (+/-)-565OK72VNFIACT
STEARIC ACID4ELV7Z65APIACT
LIMONENE, (+)-GFD7C86Q1WIACT
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 Sensitive Skin Antiperspirant Deodorant Roll-onALUMINUM CHLOROHYDRATEDistribuidora Comercial Jafra, S.A. de C.V.0d9b13ff-cd3f-477b-bda4-40e1076584b32025-01-02WarningsExact identifier
ndc (package): 68828-705-02
ndc (package): 68828-705-01
ndc (product): 68828-705
ndc11 (package): 68828070501
ndc11 (package): 68828070502
spl id: 2abdca50-ffcb-8c36-e063-6394a90af766
spl set id: 0d9b13ff-cd3f-477b-bda4-40e1076584b3

Reported adverse events (FAERS/openFDA)#

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