FDA.reportPublic FDA data

Old Spice Clinical Sweat Defense Pure Sport Plus Soft

Manufacturer
The Procter & Gamble Manufacturing Company
Effective date
2020-12-15
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:02:03

Label at a glance#

ProductOld Spice Clinical Sweat Defense Pure Sport Plus Soft
Active ingredientALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY
Label structure10 sections

Dosage and administration

apply to underarms only apply 3-4 clicks of product to underarms at bedtime rub until clear

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum zirconium trichlorohydrex Gly 15% (anhydrous)

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Use

INDICATIONS & USAGE SECTION

reduces underarm wetness

Warnings

WARNINGS SECTION

For external use only.

OTC - DO NOT USE SECTION

Do not use on broken skin

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have kidney disease

OTC - STOP USE SECTION

Stop use if rash or irritation occurs

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
  • apply 3-4 clicks of product to underarms at bedtime
  • rub until clear

Inactive ingredients

INACTIVE INGREDIENT SECTION

Cyclopentasiloxane, tribehenin, dimethicone, petrolatum, cyclodextrin, fragrance, C18-36 acid triglyceride, PPG-14 butyl ether, panthenyl triacetate

Questions?

OTC - QUESTIONS SECTION

1-800-677-7582

SPL UNCLASSIFIED SECTION

Dist. by PROCTER & GAMBLE,
CINCINNATI, OH 45202.

PRINCIPAL DISPLAY PANEL - 48 g CARTON

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Old Spice®

CLINICAL

SWEAT⋆DEFENSE

PURE SPORT PLUS

SOFT SOLID

ANTI-PERSPIRANT/
DEODORANT

ALUMINUM ZIRCONIUM
TRICHLOROHYDREX GLY

NET WT. 1.7 OZ (48 g)

OSOS

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69423-51769423-517-48

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
DIMETHICONE92RU3N3Y1OIACT
CYCLOMETHICONE 50THT5PCI0RIACT
PETROLATUM4T6H12BN9UIACT
TRIBEHENIN8OC9U7TQZ0IACT
PPG-14 BUTYL ETHERR199TJT95TIACT
ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLYT27D6T99LHACTIB
C18-36 ACID TRIGLYCERIDEZRA72DR3R7IACT
PANTHENOL TRIACETATE, (+)-1206E8961BIACT
BETADEXJV039JZZ3AIACT

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
b68200b3-b8b8-4164-e053-2995a90abefcb6761af0-2947-a420-e053-2a95a90aa0052020-12-15WarningsExact identifier
spl id: b68200b3-b8b8-4164-e053-2995a90abefc
spl set id: b6761af0-2947-a420-e053-2a95a90aa005

Reported adverse events (FAERS/openFDA)#

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