FDA.reportPublic FDA data

Black Suede

Manufacturer
New Avon LLC | Fareva Morton Grove Inc.
Effective date
2019-01-01
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 22:58:56

Label at a glance#

ProductBlack Suede Roll-On Anti-Perspirant Deodorant
Active ingredientALUMINUM CHLOROHYDRATE
Label structure7 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient      
Aluminum Chlorohydrate
14.5%, anhydrous...........

OTC - PURPOSE SECTION

           Purpose
.............Antiperspirant

INDICATIONS & USAGE SECTION

Uses
• reduces underarm perspiration
• lasts 24 hours

WARNINGS SECTION

Warnings
For external use only

OTC - WHEN USING SECTION

When using this product
• do not apply to broken skin
• stop use if rash or irritation develops

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
right away.

DOSAGE & ADMINISTRATION SECTION

Directions
• apply to underarms only

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS :
WATER/EAU, STEARETH-2,
PPG-15 STEARYL ETHER,
DICAPRYL ADIPATE, PARFUM/
FRAGRANCE, STEARETH-20,
ISOPROPYL PALMITATE.

OTC - QUESTIONS SECTION

Questions? Call 1-800-FOR-AVON
or 1-800-265-AVON in Canada

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of PDPimage of PDPimage of labelimage of labelimage of labelimage of label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
10096-9182-12022-01-28C16284748780-1d6a99b39-d1c1-a426-e053-dadaa90af4c2Black Suede Anti-Perspirant Roll-On Deodorant
10096-9182-22022-01-28C16284748780-1d6a99b39-d1c1-a426-e053-dadaa90af4c2Black Suede Anti-Perspirant Roll-On Deodorant

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10096-9182-1Black SuedeRoll-On Anti-Perspirant Deodorant50 mL in 1 BOTTLE, DISPENSINGGEL504
10096-9182-2Black SuedeRoll-On Anti-Perspirant Deodorant75 mL in 1 BOTTLE, DISPENSINGGEL754

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10096-9182BLACK SUEDE ROLL-ON ANTI-PERSPIRANT DEODORANT (ALUMINUM CHLOROHYDRATE) GEL [NEW AVON LLC]4Legacy NDC, 2 package rows20190323_74b80b23-64f5-40b2-adb7-35dab1ea7716.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ALUMINUM CHLOROHYDRATEACTIVE INGREDIENTHPN8MZW13M1
Aluminum CationACTIVE MOIETY3XHB1D032B1
ISOPROPYL PALMITATEINACTIVE INGREDIENT8CRQ2TH63M1
STEARETH-2INACTIVE INGREDIENTV56DFE46J51
STEARETH-20INACTIVE INGREDIENTL0Q8IK9E081
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10096-918210096-9182-1, 10096-9182-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ALUMINUM CHLOROHYDRATEHPN8MZW13MACTIB

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 · 13 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
ISOPROPYL PALMITATEISOPROPYL PALMITATE8CRQ2TH63MFILM / TRANSDERMAL2 mgExact identifier — unii candidate
8 equally ranked IID candidates
ISOPROPYL PALMITATEISOPROPYL PALMITATE8CRQ2TH63MGEL / TOPICALNAExact identifier — unii candidate
8 equally ranked IID candidates
ISOPROPYL PALMITATEISOPROPYL PALMITATE8CRQ2TH63MAEROSOL / TOPICAL397 mgExact identifier — unii candidate
8 equally ranked IID candidates
ISOPROPYL PALMITATEISOPROPYL PALMITATE8CRQ2TH63MAEROSOL, SPRAY / TOPICAL397 mgExact identifier — unii candidate
8 equally ranked IID candidates
STEARETH-2STEARETH-2V56DFE46J5CREAM / TOPICAL643 mgExact identifier — unii candidate
4 equally ranked IID candidates
STEARETH-20STEARETH-20L0Q8IK9E08CREAM / TOPICAL4.15 %w/wExact identifier — unii candidate
STEARETH-2STEARETH-2V56DFE46J5AEROSOL, FOAM / TOPICAL1.09 %w/wExact identifier — unii candidate
4 equally ranked IID candidates
STEARETH-2STEARETH-2V56DFE46J5OINTMENT / TOPICAL714 mgExact identifier — unii candidate
4 equally ranked IID candidates
STEARETH-2STEARETH-2V56DFE46J5LOTION / TOPICAL0.4 %w/wExact identifier — unii candidate
4 equally ranked IID candidates
ISOPROPYL PALMITATEISOPROPYL PALMITATE8CRQ2TH63MFILM, EXTENDED RELEASE / TRANSDERMAL187.5 mgExact identifier — unii candidate
8 equally ranked IID candidates
ISOPROPYL PALMITATEISOPROPYL PALMITATE8CRQ2TH63MCREAM / TOPICAL112 mgExact identifier — unii candidate
8 equally ranked IID candidates
ISOPROPYL PALMITATEISOPROPYL PALMITATE8CRQ2TH63MOINTMENT / TOPICALNAExact identifier — unii candidate
8 equally ranked IID candidates
ISOPROPYL PALMITATEISOPROPYL PALMITATE8CRQ2TH63MLOTION / TOPICAL5 %w/wExact identifier — unii candidate
8 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
84b043f9-b69c-6e89-e053-2991aa0a490274b80b23-64f5-40b2-adb7-35dab1ea77162019-01-01WarningsExact identifier
spl id: 84b043f9-b69c-6e89-e053-2991aa0a4902
spl set id: 74b80b23-64f5-40b2-adb7-35dab1ea7716

Reported adverse events (FAERS/openFDA)#

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