Oscar

Manufacturer
Prime Enterprises, Inc.
Effective date
2020-05-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:31:53

Label at a glance#

ProductOscar Anti Perspirant Deodorant
Active ingredientALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY
Label structure7 sections

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY 20%

Purpose

OTC - PURPOSE SECTION

Anti-Perspirant

INDICATIONS & USAGE SECTION

Use: Reduces underarm perspiration

WARNINGS SECTION

Warnings: For external use only.

OTC - DO NOT USE SECTION

Do not use on damaged or broken skin. Stop use if rash or irritation occurs. Ask a doctor before use if you have kidney disease.

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

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Cyclopentasiloxane, Behenyl Alcohol, Mineral Oil, Stearyl Alcohol, C10-18 Triglycerides, PEG-8 Distearate, Fragrance, Hydrogenated Castor Oil, Ethylhexyl Palmitate, Tribehenin, Glyceryl Stearate, Talc, PEG-100 Stearate

PRINCIPAL DISPLAY PANEL - 75 g Stick Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL - 75 g Stick LabelPRINCIPAL DISPLAY PANEL - 75 g Stick Label

Oscar

ANTI-PERSPIRANT DEODORANT

DÉODORANT ANTI-PERSPIRANT

NET Wt. 2.5 oz. 75g e

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
58443-032058443-0320-3

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
a563ad5a-8af8-10c0-e053-2a95a90ab7c7a563adf5-baac-8fa5-e053-2995a90a50992020-05-11WarningsExact identifier
spl id: a563ad5a-8af8-10c0-e053-2a95a90ab7c7
spl set id: a563adf5-baac-8fa5-e053-2995a90a5099

Reported adverse events (FAERS/openFDA)#

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