Dry Idea Antiperspirant Gel - Powder Fresh

Manufacturer: Henkel Corporation | VVF ILLINOIS SERVICES LLC
Effective date: 2020-02-12
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:03:43

Label at a glance#

ProductDry Idea Antiperspirant

Active ingredientALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY

Label structure9 sections

Dosage and administration

Apply to underarms only.

Storage and handling

Do not freeze or store above 105⁰F

Contacts and useful links#

PhoneLabel contact1-800-258-DIAL

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum Zirconium Octachlorohydrex GLY 16.4%

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Use

INDICATIONS & USAGE SECTION

• Reduces underarm perspiration • Extra effective

Warnings

WARNINGS SECTION

For external use only. Do not use on broken skin.

Stop use and ask a doctor

OTC - STOP USE SECTION

if rash or irritation 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.

Ask a doctor before use if

OTC - ASK DOCTOR SECTION

you have kidney disease.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply to underarms only.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aqua (Water, Eau) • Aluminum Zirconium Octachlorohydrex GLY • Alcohol Denat. • Cyclomethicone • Propylene Glycol • Dimethicone • Calcium Chloride • Trisiloxane • PEG/PPG-18/18 Dimethicone • TButyl Alcohol

STORAGE AND HANDLING SECTION

Do not freeze or store above 105⁰F

OTC - QUESTIONS SECTION

Questions? 1-800-258-DIAL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

54340-291-54 (3oz - 1970545 FL)

54340-291-54 (3oz - 1970546 BL)

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
54340-291-54	2023-01-30	C162847	48780-1	f386c64a-1296-0266-e053-dadaa90a7c1a	Dry Idea Antiperspirant Gel - Powder Fresh

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
54340-291-54	Dry Idea Antiperspirant	85 g in 1 CANISTER	GEL	85		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
54340-291	DRY IDEA ANTIPERSPIRANT (DRY IDEA CLEAR GEL ANTIPERSPIRANT - POWDER FRESH) GEL [HENKEL CORPORATION]	1	Legacy NDC, 1 package rows	20200213_9e616789-ba66-2872-e053-2a95a90a696d.zip

Products#

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

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

Dry Idea Antiperspirant
Dry Idea Clear Gel Antiperspirant - Powder Fresh
WATER
ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
54340-291	54340-291-54

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY	P9D3YP29MY	ACTIB

Source Document#

Source XML · Source PDF

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
9e616789-ba67-2872-e053-2a95a90a696d			9e616789-ba66-2872-e053-2a95a90a696d	2020-02-12	Warnings	Exact identifier spl id: 9e616789-ba67-2872-e053-2a95a90a696d spl set id: 9e616789-ba66-2872-e053-2a95a90a696d

Reported adverse events (FAERS/openFDA)#

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