Odorono

Manufacturer
Omega & Delta Co
Effective date
2024-11-19
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:38:03

Label at a glance#

ProductOdorono Antiperspirant and Deodorant Roll-on Powder
Active ingredientALUMINUM CHLOROHYDRATE
Label structure14 sections

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

USO: Reduce la humedad en las axilas. PRECAUCIONES: Solo para uso externo. No usar sobre piel irritada o lastimada. Detenga su uso si presenta irritación o alguna molestia. Consulte a su medico antes de usar. Mantengase fuera del alcance de los niños. INSTRUCCIONES DE USO: Aplique unicamente en las axilas. INGREDIENTE ACTIVO: Clorohidrato de aluminio OTROS INGREDIENTES: Agua, PPG-15 estearil éter, Estearet-2, Estearet-21, Fragancia, EDTA disódico, BHT, Triclosán. 

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Aluminum Chlorohydrate 20%

Purpose

OTC - PURPOSE SECTION

Antiperspirant

INDICATIONS & USAGE SECTION

Use: Reduces underarm wetness

WARNINGS SECTION

Warnings: For external use only

OTC - DO NOT USE SECTION

Do not use on broken skin

OTC - STOP USE SECTION

Stop use if rash or irritation occurs

OTC - ASK DOCTOR SECTION

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.

DOSAGE & ADMINISTRATION SECTION

Directions:  Apply evenly to underarms only

INACTIVE INGREDIENT SECTION

Inactive Ingredients:  Water, PPG-15 Stearyl Ether, Steareth-2, Steareth-21, Fragrance, Disodium EDTA, BHT, Triclosan

SPL UNCLASSIFIED SECTION

Hecho en Puerto Rico por:

Omega & Delta Co., Inc.

P.O. Box 1831, Carolina, P.R. 00984

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Odorono Powder FreshOdorono Powder FreshOdorono Powder FreshOdorono Powder Fresh

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51048-202-252020-11-12C16284748780-19d75b9d0-5122-f424-e053-dadaa90a57ceOdorono Antiperspirant Deodorant Roll-on Powder
51048-202-252020-01-31C16284748780-19d75b9d0-5122-f424-e053-dadaa90a57ceOdorono Antiperspirant Deodorant Roll-on Powder

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51048-202-25OdoronoAntiperspirant and Deodorant Roll-on Powder74 mL in 1 BOTTLE, WITH APPLICATORLIQUID743

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51048-202ODORONO ANTIPERSPIRANT AND DEODORANT ROLL-ON POWDER (ALUMINUM CHLOROHYDRATE) LIQUID [OMEGA & DELTA CO]3Legacy NDC, 1 package rows20241121_38d4f89f-01c6-499c-8687-010a0dabc1c8.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51048-20251048-202-25

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
2e6c6864-d8d7-487d-b3cc-01cd675d121138d4f89f-01c6-499c-8687-010a0dabc1c82024-11-19WarningsExact identifier
spl id: 2e6c6864-d8d7-487d-b3cc-01cd675d1211
spl set id: 38d4f89f-01c6-499c-8687-010a0dabc1c8

Reported adverse events (FAERS/openFDA)#

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