FDA.reportPublic FDA data

MDS Roll-On Anti-Perspirant

Manufacturer
MDS GLOBAL FZE
Effective date
2025-11-10
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:43:07

Label at a glance#

ProductMDS Roll-On Anti-Perspirant
Active ingredientALUMINUM CHLOROHYDRATE ANHYDROUS
Label structure8 sections

Indications and uses

reduces underarm perspiration

Dosage and administration

apply to underarms only

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum Chlorohydrate, 15.4 % anhydrous

Purpose

OTC - PURPOSE SECTION

Anti-Perspirant Deodorant

Uses

INDICATIONS & USAGE SECTION

reduces underarm perspiration

Warnings

WARNINGS SECTION

  • For external use only 
  • Do not apply to broken skin. Stop use if rash or irritation occurs. 
  • Ask a doctor before use if you have kidney disease. 
  • 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 ingredients

INACTIVE INGREDIENT SECTION

DIMETHICONOL, FRAGRANCE, ISOPROPYL MYRISTATE, STEARETH-2, STEARETH-20, WATER.

Other information

SPL UNCLASSIFIED SECTION

Helps eliminate odor - Anti-stain -Non-stinging. - Non-sticky - Quick-drying

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87119-001-01MDS Roll-On Anti-Perspirant50 mL in 1 BOTTLECREAM501

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87119-00187119-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
STEARETH-2V56DFE46J5IACT
STEARETH-20L0Q8IK9E08IACT
WATER059QF0KO0RIACT
DIMETHICONE, UNSPECIFIED92RU3N3Y1OIACT
ALUMINUM CHLOROHYDRATE ANHYDROUS407PSC3OC7ACTIB

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
MDS Roll-On Anti-PerspirantALUMINUM CHLOROHYDRATEMDS GLOBAL FZE501eedce-9dcc-4def-ba5b-e97cad0e1e762025-11-10WarningsExact identifier
ndc (package): 87119-001-01
ndc (product): 87119-001
ndc11 (package): 87119000101
spl id: 4340f1c6-a2eb-b885-e063-6394a90a0cae
spl set id: 501eedce-9dcc-4def-ba5b-e97cad0e1e76

Reported adverse events (FAERS/openFDA)#

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