Imari Blossom

Manufacturer
Avon Products, Inc
Effective date
2012-10-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:33:23

Label at a glance#

ProductImari Blossom 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

WARNINGS SECTION

Warnings

For external use only

OTC - DO NOT USE SECTION

Do not use on broken skin

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have kidney disease

OTC - STOP USE SECTION

Stop use if rash or irritation occurs

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 PDP

SPL UNCLASSIFIED SECTION

image of DFBimage of DFB

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
10096-0286-12019-11-27C16284748780-19855d018-e048-cd31-e053-dbdaa90ab51a04ac8c94-4e6a-4501-9b97-c1f9307a6c73

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10096-0286-1Imari BlossomRoll-on Anti-perspirant Deodorant50 mL in 1 BOTTLE, DISPENSINGGEL501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10096-0286IMARI BLOSSOM ROLL-ON ANTI-PERSPIRANT DEODORANT (ALUMINUM CHLOROHYDRATE) GEL [AVON PRODUCTS, INC]1Legacy NDC, 1 package rows20121026_04ac8c94-4e6a-4501-9b97-c1f9307a6c73.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
Aluminum ChlorohydrateACTIVE INGREDIENTHPN8MZW13M1
ALUMINUM CHLOROHYDRATEACTIVE MOIETYHPN8MZW13M1

Products#

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

DailyMed product names page 1 of 1 · 2 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10096-028610096-0286-1

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
Aluminum ChlorohydrateHPN8MZW13MACTIM

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
e3f82075-c54f-4ded-ae1b-562849dba2d004ac8c94-4e6a-4501-9b97-c1f9307a6c732012-10-17WarningsExact identifier
spl id: e3f82075-c54f-4ded-ae1b-562849dba2d0
spl set id: 04ac8c94-4e6a-4501-9b97-c1f9307a6c73

Reported adverse events (FAERS/openFDA)#

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