FDA.reportPublic FDA data

Harrys Extra Strength Antiperspirant Shiso

Manufacturer
Harry's Inc.
Effective date
2024-12-20
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 20:44:54

Label at a glance#

ProductHarrys Extra Strength Antiperspirant Shiso
Active ingredientALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ALUMINUM ZIRCONIIUM TRICHLOROHYDREX GLY 20%

OTC - PURPOSE SECTION

Purpose. Antiperspirant

INDICATIONS & USAGE SECTION

Reduces underarm wetness. Extra effective.

WARNINGS SECTION

For external use only

OTC - DO NOT USE SECTION

Do not use on broken skin

OTC - ASK DOCTOR SECTION

Ask doctor if before use if you have kidney disease.

OTC - STOP USE SECTION

Stop use if rash or itrritation 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.

DOSAGE & ADMINISTRATION SECTION

Directions

  • Apply to underarms only
  • Apply at bedtime

INACTIVE INGREDIENT SECTION

STEARYL ALCOHOL, DIMETHICONE, C15-19 ALKANE, DIHEPTYL SUCCINATE, WATER/AQUA/EAU, C12-15 ALKYL BENZOATE, HYDROGENATED CASTOR OIL, CETYL ALCOHOL, SILICA, FRAGRANCE/PARFUM, ALUMINUM STARCH OCENTYLSUCCINATE, SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL, ALLANTOIN, BISABOLOL, ZINGIBER OFFINCALE (GINGER) ROOT EXTRACT, TOCOPHERYL ACETATE, MYRISTYL aLCOHOL, CITRONELLYL METHYLCROTONATE, CAPRYLOYL GLYCERIN/SEBACIC ACID COPOLYMER, LIMONENE, HEXYL CINNAMAL, LINALOOL, BENZYL ALCOHOL, EUGENOL, CITRAL.

Questions?

OTC - QUESTIONS SECTION

1-888-212-6855

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

L2 Shiso frontL2 Shiso front

l3 shiso backl3 shiso back

NDC 70533-010-25

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70533-010HARRYS EXTRA STRENGTH ANTIPERSPIRANT SHISO (ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY) STICK [HARRY'S INC.]5Legacy NDC20241222_adcb1ca7-bdd3-8981-e053-2a95a90a6dec.zip

Products#

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

DailyMed product names page 1 of 1 · 27 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70533-01070533-010-25

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 26 matching rows.

Name, UNII, Kind table
NameUNIIKind
DIHEPTYL SUCCINATE057N7SS26YIACT
C15-19 ALKANECI87N1IM01IACT
FRAGRANCE 135765EM498GW35IACT
CITRONELLYL METHYLCROTONATEK61O222P3DIACT
LINALOOL, (+/-)-D81QY6I88EIACT
CAPRYLOYL GLYCERIN/SEBACIC ACID COPOLYMER (2000 MPA.S)N7YC58165TIACT
WATER059QF0KO0RIACT
CETYL ALCOHOL936JST6JCNIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
ALUMINUM STARCH OCTENYLSUCCINATEI9PJ0O6294IACT
GINGERC5529G5JPQIACT
BENZYL ALCOHOLLKG8494WBHIACT
EUGENOL3T8H1794QWIACT
DIMETHICONE92RU3N3Y1OIACT
HYDROGENATED CASTOR OILZF94AP8MEYIACT
ALKYL (C12-15) BENZOATEA9EJ3J61HQIACT
STEARYL ALCOHOL2KR89I4H1YIACT
JOJOBA OIL724GKU717MIACT
.ALPHA.-BISABOLOL, (+/-)-36HQN158VCIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
MYRISTYL ALCOHOLV42034O9PUIACT
ALLANTOIN344S277G0ZIACT
LIMONENE, (+/-)-9MC3I34447IACT
ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLYT27D6T99LHACTIB
.ALPHA.-HEXYLCINNAMALDEHYDE7X6O37OK2IIACT
CITRALT7EU0O9VPPIACT

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
463e90de-dd8a-0d2b-e063-6294a90ad254adcb1ca7-bdd3-8981-e053-2a95a90a6dec2025-12-18WarningsExact identifier
spl set id: adcb1ca7-bdd3-8981-e053-2a95a90a6dec

Reported adverse events (FAERS/openFDA)#

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