Harrys Antiperspirant Redwood

Manufacturer
Harry's Inc.
Effective date
2024-12-20
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 20:44:54

Label at a glance#

ProductHarrys Antiperspirant Redwood
Active ingredientALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY
Label structure8 sections

Dosage and administration

Apply to underarms only

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

ALUMINUM ZIRCONIIUM TRICHLOROHYDREX GLY 16%

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Use

INDICATIONS & USAGE SECTION

Reduces underarm wetness

Warnings

WARNINGS SECTION

For external Use only

OTC - DO NOT USE SECTION

Do not use on broken skin

OTC - ASK DOCTOR SECTION

Ask doctor before use if you have kidney disease

OTC - STOP USE SECTION

Stop use 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.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply to underarms only

Inactive Ingredients

INACTIVE INGREDIENT SECTION

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

OTC - QUESTIONS SECTION

Questions?: 1-888-212-6855

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

l2 redwood frontl2 redwood frontl2 redwood backl2 redwood back

NDC: 70533-008-25

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70533-008HARRYS ANTIPERSPIRANT REDWOOD (ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY) STICK [HARRY'S INC.]4Legacy NDC20241222_adcaa63c-423c-9076-e053-2995a90aa308.zip

Products#

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

DailyMed product names page 1 of 1 · 26 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70533-00870533-008-25

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 25 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
463e76c5-6c0f-8337-e063-6394a90a3075adcaa63c-423c-9076-e053-2995a90aa3082025-12-18WarningsExact identifier
spl set id: adcaa63c-423c-9076-e053-2995a90aa308

Reported adverse events (FAERS/openFDA)#

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