FDA.reportPublic FDA data

Soft and Dri Clinical Protection

Manufacturer
VVF Kansas Services LLC
Effective date
2021-11-17
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:26:53

Label at a glance#

ProductSoft and Dri Clinical Protection Fresh Pomegranate
Active ingredientALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY
Label structure14 sections

Dosage and administration

apply to underarms only

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum Zirconium Trichlorohydrex Gly 20%

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Use

INDICATIONS & USAGE SECTION

reduces underarm perspiration

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 and ask a doctor if rash or irration occurs

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

Cyclopentasiloxane, Stearyl Alcohol, Isopropyl Palmitate, PPG-14 Butyl Ether,

Hydrogenated Castor Oil, Fragrance, Glyceryl Stearate, PEG-100 Stearate,

C12-15 Alkyl Benzoate, Phenyl Trimethicone

OTC - QUESTIONS SECTION

1-800-699-6852

softndri.com

SPL UNCLASSIFIED SECTION

Manufactured in USA

Distributed by The Village Company ®

Eden Praire, MN 55344

SPL UNCLASSIFIED SECTION

Soft & Dri Clinical

Fresh Pomegranate

antiperspirant deodorant

max level wetness protection

Maximum strength odor and wetness blocking technology with body-responsive fragrance capsules for all-day freshness

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Soft Dri Clinical LabelsSoft Dri Clinical Labels

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10889-42510889-425-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
PPG-14 BUTYL ETHERR199TJT95TIACT
PHENYL TRIMETHICONEDR0K5NOJ4RIACT
STEARYL ALCOHOL2KR89I4H1YIACT
ISOPROPYL PALMITATE8CRQ2TH63MIACT
ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLYT27D6T99LHACTIB
CYCLOMETHICONE 50THT5PCI0RIACT
HYDROGENATED CASTOR OILZF94AP8MEYIACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
PEG-100 STEARATEYD01N1999RIACT
ALKYL (C12-15) BENZOATEA9EJ3J61HQIACT

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
d0fd7514-f489-7949-e053-2a95a90a931d5fafa80f-b815-3540-e053-2a91aa0a55de2021-11-17WarningsExact identifier
spl id: d0fd7514-f489-7949-e053-2a95a90a931d
spl set id: 5fafa80f-b815-3540-e053-2a91aa0a55de

Reported adverse events (FAERS/openFDA)#

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