FDA.reportPublic FDA data

Obao Men Audaz

Manufacturer
ALL NATURAL DYNAMICS | Cosbel S.A de C.V.
Effective date
2013-08-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:36:46

Label at a glance#

ProductObao Men Audaz
Active ingredientALUMINUM CHLOROHYDRATE
Label structure6 sections

Indications and uses

Reduces underarm perspective

Dosage and administration

Apply to underarms only

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum Chlorohydrate 15%

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Uses

INDICATIONS & USAGE SECTION

Reduces underarm perspective

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

in broken skin

Stop use if

OTC - STOP USE SECTION

rash or irritation occurs

Ask a doctor

OTC - ASK DOCTOR SECTION

before use if you have kidney disease

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

water, corn starch, cetearyl alcohol, fragrance, dimethicone, linalool, alpha-isomethyl ionone, geraniol, ceteareath-33, butylphenyl methylpropional, citronellol.

Product Labeling

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51769-888-652019-11-27C16284748780-19855d018-d775-cd31-e053-dbdaa90ab51aObao Men Audaz (Men Oceanic)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51769-888-65Obao Men Audaz65 g in 1 BOTTLE, WITH APPLICATORLIQUID651

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51769-888OBAO MEN AUDAZ (ALUMINUM CHLOROHYDRATE) LIQUID [ALL NATURAL DYNAMICS]1Legacy NDC, 1 package rows20130831_844b7587-1bb8-44a7-b6a0-17ac36a51b07.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ALUMINUM CHLOROHYDRATEACTIVE INGREDIENTHPN8MZW13M1
ALUMINUM CHLOROHYDRATEACTIVE MOIETYHPN8MZW13M1
.BETA.-CITRONELLOL, (R)-INACTIVE INGREDIENTP01OUT964K1
BUTYLPHENYL METHYLPROPIONALINACTIVE INGREDIENTT7540GJV691
CETEARETH-33INACTIVE INGREDIENTR42C2O714B1
CETOSTEARYL ALCOHOLINACTIVE INGREDIENT2DMT128M1S1
DIMETHICONEINACTIVE INGREDIENT92RU3N3Y1O1
GERANIOLINACTIVE INGREDIENTL837108USY1
ISOMETHYL-.ALPHA.-IONONEINACTIVE INGREDIENT9XP4LC555B1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51769-88851769-888-65

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALUMINUM CHLOROHYDRATEHPN8MZW13MACTIB
WATER059QF0KO0RIACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
DIMETHICONE92RU3N3Y1OIACT
ISOMETHYL-.ALPHA.-IONONE9XP4LC555BIACT
GERANIOLL837108USYIACT
CETEARETH-33R42C2O714BIACT
BUTYLPHENYL METHYLPROPIONALT7540GJV69IACT
.BETA.-CITRONELLOL, (R)-P01OUT964KIACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 9 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
CETOSTEARYL ALCOHOLCETOSTEARYL ALCOHOL2DMT128M1SOINTMENT / TOPICAL1.2 %w/wExact identifier — unii candidate
9 equally ranked IID candidates
CETOSTEARYL ALCOHOLCETOSTEARYL ALCOHOL2DMT128M1SSPRAY / TOPICAL1 %w/wExact identifier — unii candidate
9 equally ranked IID candidates
CETOSTEARYL ALCOHOLCETOSTEARYL ALCOHOL2DMT128M1SLOTION / TOPICAL3627 mgExact identifier — unii candidate
9 equally ranked IID candidates
CETOSTEARYL ALCOHOLCETOSTEARYL ALCOHOL2DMT128M1SAEROSOL, FOAM / TOPICAL21 mgExact identifier — unii candidate
9 equally ranked IID candidates
CETOSTEARYL ALCOHOLCETOSTEARYL ALCOHOL2DMT128M1SCREAM / TOPICAL1428 mgExact identifier — unii candidate
9 equally ranked IID candidates
CETOSTEARYL ALCOHOLCETOSTEARYL ALCOHOL2DMT128M1SSUPPOSITORY / VAGINALNAExact identifier — unii candidate
9 equally ranked IID candidates
CETOSTEARYL ALCOHOLCETOSTEARYL ALCOHOL2DMT128M1SCREAM / VAGINAL6 mgExact identifier — unii candidate
9 equally ranked IID candidates
CETOSTEARYL ALCOHOLCETOSTEARYL ALCOHOL2DMT128M1SCAPSULE, EXTENDED RELEASE / ORAL9.43 mgExact identifier — unii candidate
9 equally ranked IID candidates
CETOSTEARYL ALCOHOLCETOSTEARYL ALCOHOL2DMT128M1STABLET, EXTENDED RELEASE / ORAL800 mgExact identifier — unii candidate
9 equally ranked IID candidates

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
ffb56df0-1f94-4f1f-8703-ffd2cc905587844b7587-1bb8-44a7-b6a0-17ac36a51b072013-08-23WarningsExact identifier
spl id: ffb56df0-1f94-4f1f-8703-ffd2cc905587
spl set id: 844b7587-1bb8-44a7-b6a0-17ac36a51b07

Reported adverse events (FAERS/openFDA)#

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