Dry Idea AD Antiperspirant Roll-On Powder Fresh

Manufacturer
KDC/ONE Development Corporation, Inc
Effective date
2021-08-18
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 22:38:13

Label at a glance#

ProductDry Idea AD Antiperspirant Roll-On Powder Fresh
Active ingredientALUMINUM ZIRCONIUM PENTACHLOROHYDREX GLY
Label structure13 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Aluminum Zirconium Pentachlorohydrex Gly 16.3%

OTC - PURPOSE SECTION

USE:  Reduces underarm perspiration.  Extra effective

WARNINGS SECTION

Warnings.....For external use only.

OTC - DO NOT USE SECTION

Do not use on broken skin.

OTC - STOP USE SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have kidney disease.

INDICATIONS & USAGE SECTION

Directions:  Shake well.  Apply to underarms only.

INACTIVE INGREDIENT SECTION

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

OTC - QUESTIONS SECTION

Questions:  1-800-258-DIAL

HOW SUPPLIED SECTION

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

DOSAGE & ADMINISTRATION SECTION

DIRECTIONS: Shake well. Apply to underarms only.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DI_PwFr

DI_PwFrDI_PwFr

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
54565-290154565-2901-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
c9dac443-38cb-e717-e053-2a95a90a9abf9622dc99-7c78-1422-e053-2995a90a16632021-08-18WarningsExact identifier
spl id: c9dac443-38cb-e717-e053-2a95a90a9abf
spl set id: 9622dc99-7c78-1422-e053-2995a90a1663

Reported adverse events (FAERS/openFDA)#

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