DRY IDEA STRESS SHIELD INSPIRE ANTIPERSPIRANT DEODORANT ROLL-ON- aluminum zirconium pentachlorohydrex gly liquid
KDC/ONE Development Corporation, Inc

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Dry Idea Stress Shield Inspire Roll-On Antiperspirant and Deodorant

Aluminum Zirconium Pentachlorohydrex Gly 16.3%

USE....Reduces underarm perspiration - Extra effective

Warnings...For external use only.

Do not use on broken skin.

Stop use and ask a doctor is rash or irritation occurs.

Keep out of reach of children. If swallowed, get medical help or contact a poison control center right away.

Ask a doctor before use if you have kidney disease.

Directions: Shake well. Apply to underarms only.

Inactive Ingredients; Cyclomethicone, Disteardimonium Hectorite, Propylene Carbonate, Gossypium Herbaceum (Cotton) Seed Oil, Tocopheryl Acetate (Vitamin E Acetate), Isopropyl Myristate, Fragrance, Zea Mays (Corn) Starch.

Questions: 1-800-258-DIAL

2017 Distributed By The Dial Corporation, Scottsdale, AZ 85255. Henkel Corporation, Rocky Hill, CT 06067.

DIRECTIONS: Shake well. Apply to underarms only.

DI_Inspire

DRY IDEA STRESS SHIELD INSPIRE ANTIPERSPIRANT DEODORANT ROLL-ON
aluminum zirconium pentachlorohydrex gly liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:54565-2904
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALUMINUM ZIRCONIUM PENTACHLOROHYDREX GLY (UNII: 94703016SM) (ALUMINUM ZIRCONIUM PENTACHLOROHYDREX GLY - UNII:94703016SM)	ALUMINUM ZIRCONIUM PENTACHLOROHYDREX GLY	16.3 g in 96.1 mL

Ingredient Name	Strength
Inactive Ingredients
DIPROPYLENE GLYCOL (UNII: E107L85C40)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
TOCOPHEROL (UNII: R0ZB2556P8)
PPG-14 BUTYL ETHER (UNII: R199TJT95T)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:54565-2904-1	96.1 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product	10/30/2019

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part350	10/07/2014

Labeler - KDC/ONE Development Corporation, Inc (204006464)

Name	Address	ID/FEI	Business Operations
Establishment
KDC/ONE Development Corporation, Inc		204006464	manufacture(54565-2904) , analysis(54565-2904) , pack(54565-2904) , label(54565-2904)

Revised: 8/2021

Document Id: c9dac443-38d0-e717-e053-2a95a90a9abf

Set id: 9622edff-cf25-90fc-e053-2a95a90ad4a2

Version: 4

Effective Time: 20210818

KDC/ONE Development Corporation, Inc