Soft and Dri Cool and Clean

Manufacturer
The Village Company | Apex International | KIK
Effective date
2019-12-17
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:02:02

Label at a glance#

ProductSoft and Dri Soft Scent
Active ingredientALUMINUM CHLOROHYDRATE
Label structure19 sections

Dosage and administration

Shake Well. Apply to underarms only.

Label contents#

Full prescribing information#

SOFT & DRI

OTC - ACTIVE INGREDIENT SECTION

  • Comfortable protection even after shaving
  • Keeps you Fresh and DRY for 24 Hours
  • Anti Stain Formual Keeps Clothes Free from Underarm Stains
  • Light, Fresh Scent Keeps You Feeling clean and Comfortable All Day

OTC - PURPOSE SECTION

Antiperspirant Deodorant

Use

INDICATIONS & USAGE SECTION

reduces underarm perspiration

Warnings For external use only

WARNINGS SECTION

Flammable

  • do not spray near flame or while smoking
  • contents under pressure; do not crush, puncture or incinerate
  • donot store at a temperature above 120 F

Do not use on broken skin

Stop use and ask a doctor if

OTC - STOP USE SECTION

rash or irritation occurs

When using this product

OTC - WHEN USING SECTION

  • use only as directed; intentional misuse by deliberately concentration and inhaling the contents can be hramful or fatal
  • avoid spraying in eyes
  • keep away from face and mouth to avoid breating it

Keep out of reach of chlidren

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a posion control center right away

Ask a doctor before use if

OTC - ASK DOCTOR/PHARMACIST SECTION

you have kidney disease

Directions

INSTRUCTIONS FOR USE SECTION

Shake Well. Apply to underarms only.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Butane, Hydofluorocarbon 152a, Cyclopentsiloxane, Cyclotetrasiloxane, Talc, Silica Dimethyl Silylate, Fragrance (Parfum), Silica, Alpha-Iso-methyl Ionone, Benzyl Salicylate, Butylphenyl Methylpropional, Eugenol, Hexyl Cinnamal

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum Chlorohyrdrate 25%

Purpose

OTC - PURPOSE SECTION

Anitperspirant

Use

INDICATIONS & USAGE SECTION

Reduces underarm perspiration

Warnings Fore external use only

WARNINGS SECTION

Flammable

  • do not spray near flame or while smoking
  • contents under pressure; do not crush, puncture or incinerate
  • donot store at a temperature above 120 F

Do not use on broken skin

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

Ask a doctor before use if

OTC - ASK DOCTOR SECTION

you have kidney disease

Stop use and ask a doctor if

OTC - STOP USE SECTION

rash or irritation occurs

When using this product

OTC - WHEN USING SECTION

  • use only as directed; intentional misuse by deliberately concentration and inhaling the contents can be hramful or fatal
  • avoid spraying in eyes
  • keep away from face and mouth to avoid breating it

Directions

INSTRUCTIONS FOR USE SECTION

Shake well. Apply to underarms only.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Butane, cylcpentasiloxane, Hydroflurocarbon 152a, Talc, Fragrance (Parfum), Silica Dimethyul Silylate, Silica, Aloe, Bardeandensis Leaf Juice Powder.

DOSAGE & ADMINISTRATION SECTION

Apply to underarms only.

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

back panel soft and dri Soft Scentback panel soft and dri Soft Scent

Aluminum Chlorohydrate 20%

Soft & Dri aerosol

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Front Soft and Dri Soft scentFront Soft and Dri Soft scent

Keeps you Fresh and Dri

For 24 Hours

Soft Scent

ANTIPERSPIRANT DEODORANT

NET WT 6.0 OZ (170 G)

Soft & Dri Cool& Clean

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Soft and Dri cool and Clean backSoft and Dri cool and Clean backSoft and Dri cool and clean frontSoft and Dri cool and clean front

drispray

clincial Protection

Aerosol

Max Level Wetness Protection

Cool & Clean

ANTIPERSPIRANT DEODORANT

NET WT 3.6 OZ (102G)

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69752-101-062023-01-30C16284748780-1f386c64a-051f-0266-e053-dadaa90a7c1a321df736-5cdf-5e6e-e054-00144ff8d46c

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69752-101-06Soft and Dri Soft Scent170 g in 1 CANAEROSOL1703
69752-103-36Soft and Dri Cool and Clean102 g in 1 CANAEROSOL1023

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69752-101SOFT AND DRI SOFT SCENT (ALUMINUM CHLOROHYDRATE) AEROSOL SOFT AND DRI COOL AND CLEAN (ALUMINUM CHLOROHYDRATE) AEROSOL [THE VILLAGE COMPANY]3Legacy NDC, 1 package rows20191218_321df736-5cdf-5e6e-e054-00144ff8d46c.zip
69752-103SOFT AND DRI SOFT SCENT (ALUMINUM CHLOROHYDRATE) AEROSOL SOFT AND DRI COOL AND CLEAN (ALUMINUM CHLOROHYDRATE) AEROSOL [THE VILLAGE COMPANY]3Legacy NDC, 1 package rows20191218_321df736-5cdf-5e6e-e054-00144ff8d46c.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69752-10169752-101-06
69752-10369752-103-36

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

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
99eda7e2-fed8-6d4b-e053-2a95a90a8fd1321df736-5cdf-5e6e-e054-00144ff8d46c2019-12-17WarningsExact identifier
spl id: 99eda7e2-fed8-6d4b-e053-2a95a90a8fd1
spl set id: 321df736-5cdf-5e6e-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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