FDA.reportPublic FDA data

Dry Idea Advanced Dry

Manufacturer
The Dial Corporation | Diversapack of Monroe
Effective date
2011-05-19
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 22:29:00

Label at a glance#

ProductDry Idea Advanced Dry
Active ingredientAluminum Zirconium Pentachlorohydrex gly
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active  Ingredient Purpose

Aluminum Zirconium Pentacholrohydrex Gly 16.3%.......Antiperspirant

OTC - PURPOSE SECTION

Antiperspirant

INDICATIONS & USAGE SECTION

Use

  • Reduces underarm perspiration
  • Extra effective

WARNINGS SECTION

Warnings for external use only.

Do not use on broken skin.

Stop use and ask a doctor if

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.

DOSAGE & ADMINISTRATION 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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL


image of dry idea labelimage of dry idea label


dry idea.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
54340-004-122019-10-29C16284748780-1960f7f55-db23-8e05-e053-dbdaa90a074aDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
54340-004-12Dry Idea Advanced Dry12 in 1 BOXLIQUID124
54340-004-32Dry Idea Advanced Dry96.1 mL in 1 BOTTLE, PLASTICLIQUID96.14

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
54340-004DRY IDEA ADVANCED DRY (ALUMINUM ZIRCONIUM PENTACHLOROHYDREX GLY ) LIQUID [THE DIAL CORPORATION]4Legacy NDC, 2 package rows20110729_be84d7b3-ec58-40da-9806-452214318b31.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
Aluminum Zirconium Pentachlorohydrex glyACTIVE INGREDIENT94703016SM4
Aluminum Zirconium Pentachlorohydrex GlyACTIVE MOIETY94703016SM4
.ALPHA.-TOCOPHEROL ACETATE, D-INACTIVE INGREDIENTA7E6112E4N4
BentoniteINACTIVE INGREDIENTA3N5ZCN45C4
CyclomethiconeINACTIVE INGREDIENTNMQ347994Z4
Propylene CarbonateINACTIVE INGREDIENT8D08K3S51E4
STEARYL MYRISTATEINACTIVE INGREDIENT310RUQ1G0W4

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
54340-00454340-004-32, 54340-004-12

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
Aluminum Zirconium Pentachlorohydrex gly94703016SMACTIM
CyclomethiconeNMQ347994ZIACT
Propylene Carbonate8D08K3S51EIACT
.ALPHA.-TOCOPHEROL ACETATE, D-A7E6112E4NIACT
STEARYL MYRISTATE310RUQ1G0WIACT
BentoniteA3N5ZCN45CIACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 17 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
BentoniteBENTONITEA3N5ZCN45CSYSTEM / TRANSDERMAL9.86 mgExact identifier — unii candidate
11 equally ranked IID candidates
BentoniteBENTONITEA3N5ZCN45CPOWDER, DENTIFRICE / DENTAL0.05 mg/mgExact identifier — unii candidate
11 equally ranked IID candidates
CyclomethiconeCYCLOMETHICONENMQ347994ZAEROSOL, FOAM / TOPICAL5.26 %w/wExact identifier — unii candidate
5 equally ranked IID candidates
BentoniteBENTONITEA3N5ZCN45CCAPSULE / ORALADJ PHExact identifier — unii candidate
11 equally ranked IID candidates
CyclomethiconeCYCLOMETHICONENMQ347994ZSOLUTION / TOPICAL11.57 %w/vExact identifier — unii candidate
5 equally ranked IID candidates
BentoniteBENTONITEA3N5ZCN45CLOTION / TOPICAL5 %w/wExact identifier — unii candidate
11 equally ranked IID candidates
BentoniteBENTONITEA3N5ZCN45CPOWDER / TOPICAL0.67 mg/mgExact identifier — unii candidate
11 equally ranked IID candidates
BentoniteBENTONITEA3N5ZCN45CSUSPENSION / ORAL65 mg/5mlExact identifier — unii candidate
11 equally ranked IID candidates
CyclomethiconeCYCLOMETHICONENMQ347994ZCREAM / TOPICAL13 %w/wExact identifier — unii candidate
5 equally ranked IID candidates
Propylene CarbonatePROPYLENE CARBONATE8D08K3S51EOINTMENT / TOPICAL3000 mgExact identifier — unii candidate
BentoniteBENTONITEA3N5ZCN45CTABLET, COATED / ORAL1.8 mgExact identifier — unii candidate
11 equally ranked IID candidates
BentoniteBENTONITEA3N5ZCN45CTABLET / ORAL355 mgExact identifier — unii candidate
11 equally ranked IID candidates
BentoniteBENTONITEA3N5ZCN45CSUPPOSITORY / VAGINAL288.1 mgExact identifier — unii candidate
11 equally ranked IID candidates
CyclomethiconeCYCLOMETHICONENMQ347994ZCREAM, AUGMENTED / TOPICAL7.6 %w/wExact identifier — unii candidate
5 equally ranked IID candidates
BentoniteBENTONITEA3N5ZCN45CCREAM / TOPICAL4.1 %w/wExact identifier — unii candidate
11 equally ranked IID candidates
CyclomethiconeCYCLOMETHICONENMQ347994ZLOTION / TOPICAL3510 mgExact identifier — unii candidate
5 equally ranked IID candidates
BentoniteBENTONITEA3N5ZCN45CSHAMPOO, SUSPENSION / TOPICAL3.25 %w/vExact identifier — unii candidate
11 equally ranked IID candidates

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
6d05f765-e802-4a5a-83f6-c690030776a7be84d7b3-ec58-40da-9806-452214318b312011-05-19WarningsExact identifier
spl id: 6d05f765-e802-4a5a-83f6-c690030776a7
spl set id: be84d7b3-ec58-40da-9806-452214318b31

Reported adverse events (FAERS/openFDA)#

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