SOFT AND DRI CLINICAL PROTECTION FRESH POMEGRANATE- aluminum zirconium trichlorohydrex gly 20% stick

Soft and Dri Clinical Protection by

Drug Labeling and Warnings

Soft and Dri Clinical Protection by is a Otc medication manufactured, distributed, or labeled by VVF Kansas Services LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Aluminum Zirconium Trichlorohydrex Gly 20%

Purpose

Antiperspirant

Use

reduces underarm perspiration

Warnings

For external use only

DO NOT USE

Do not use on broken skin

ASK DOCTOR

Ask a doctor before use if you have kidney disease

STOP USE

Stop use and ask a doctor if rash or irration occurs

Keep out of reach of children.

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

Directions

apply to underarms only

Inactive Ingredients

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

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

C12-15 Alkyl Benzoate, Phenyl Trimethicone

QUESTIONS

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SOFT AND DRI CLINICAL PROTECTION  FRESH POMEGRANATE
aluminum zirconium trichlorohydrex gly 20% stick

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10889-425
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY (UNII: T27D6T99LH) (ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY - UNII:T27D6T99LH)	ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY	20 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
PPG-14 BUTYL ETHER (UNII: R199TJT95T)
PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
PEG-100 STEARATE (UNII: YD01N1999R)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10889-425-01	65 g in 1 APPLICATOR; Type 0: Not a Combination Product	11/28/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part350	11/28/2016

Labeler - VVF Kansas Services LLC (833164242)

Registrant - VVF Kansas Services LLC (833164242)

Establishment
Name	Address	ID/FEI	Business Operations
VVF Kansas Services LLC		833164242	manufacture(10889-425)