FDA.reportPublic FDA data

Odorono

Manufacturer
Omega & Delta Co
Effective date
2026-01-21
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:34:50

Label at a glance#

ProductOdorono Antiperspirant and Deodorant Roll-on Original
Active ingredientALUMINUM CHLOROHYDRATE
Label structure13 sections

Label contents#

Full prescribing information#

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 OriginalOdorono OriginalOdorono OriginalOdorono Original

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130742699002018GTIN-13: 0742699002018
EAN-13: 0742699002018
GTIN-12: 742699002018
UPC-A: 742699002018
GTIN storage (14 digits): 00742699002018		Odorono Original.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51048-201-252020-11-12C16284748780-19d75b9d0-d4d4-f424-e053-dadaa90a57ceOdorono Antiperspirant Deodorant Roll-on Original
51048-201-252020-01-31C16284748780-19d75b9d0-d4d4-f424-e053-dadaa90a57ceOdorono Antiperspirant Deodorant Roll-on Original

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51048-201-25OdoronoAntiperspirant and Deodorant Roll-on Original74 mL in 1 BOTTLE, WITH APPLICATORLIQUID744

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
51048-20151048-201-25

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALUMINUM CHLOROHYDRATEHPN8MZW13MACTIB
WATER059QF0KO0RIACT
PPG-15 STEARYL ETHER1II18XLS1LIACT
STEARETH-2V56DFE46J5IACT
STEARETH-2153J3F32P58IACT
EDETATE DISODIUM7FLD91C86KIACT
BUTYLATED HYDROXYTOLUENE1P9D0Z171KIACT
TRICLOSAN4NM5039Y5XIACT

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
Odorono Antiperspirant and Deodorant Roll-on OriginalALUMINUM CHLOROHYDRATEOmega & Delta Co115ae61a-8dd4-43a8-9dc3-be98f710e5e22026-01-21WarningsExact identifier
ndc (package): 51048-201-25
ndc (product): 51048-201
ndc11 (package): 51048020125
spl id: cae929ea-6ae8-414e-bad1-7dd91956f131
spl set id: 115ae61a-8dd4-43a8-9dc3-be98f710e5e2

Reported adverse events (FAERS/openFDA)#

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