FDA.reportPublic FDA data

Roll On Anti-Perspirant Deodorant

Manufacturer
Keefe Group
Effective date
2026-01-08
Label type
HUMAN OTC DRUG LABEL
Version
14
Source
monthly-update
Hydrated at
2026-06-03 17:52:19

Label at a glance#

ProductRoll On Anti-Perspirant Deodorant
Active ingredientALUMINUM CHLOROHYDRATE
Label structure9 sections

Dosage and administration

Apply to underarms only.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum Chlorohydrate, 14% – Anhydrous Basis

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Use

INDICATIONS & USAGE SECTION

Reduces underarm wetness.

Warnings

WARNINGS SECTION

For external use only.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

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 havekidney disease. If swallowed, get medical help or contact a Poison Control Center immediately. Use only as directed.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply to underarms only.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Purified Water, Hydroxyethylcellulose, Glycerin, Polysorbate 20, Fragrance, Tetrasodium EDTA

SPL UNCLASSIFIED SECTION

Distributed by:
Olivette Products, L.L.C., Bridgeton, MO 63044

PRINCIPAL DISPLAY PANEL - 88 ml Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

FORCE

POWER UP
ANTI-PERSPIRANT
& DEODORANT ROLL-ON

3 fl oz/88 ml 

PRINCIPAL DISPLAY PANEL - 88 ml Bottle LabelPRINCIPAL DISPLAY PANEL - 88 ml Bottle Label

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130087381260421GTIN-13: 0087381260421
EAN-13: 0087381260421
GTIN-12: 087381260421
UPC-A: 087381260421
GTIN storage (14 digits): 00087381260421		force-power-up-01.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51870-001-03Roll On Anti-Perspirant Deodorant88 mL in 1 BOTTLE, WITH APPLICATORSOLUTION8814

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ALUMINUM CHLOROHYDRATEACTIVE INGREDIENTHPN8MZW13M1
ALUMINUM CHLOROHYDRATEACTIVE MOIETYHPN8MZW13M1
Edetate SodiumINACTIVE INGREDIENTMP1J8420LU1
GlycerinINACTIVE INGREDIENTPDC6A3C0OX1
HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%)INACTIVE INGREDIENTS38J6RZN161
Polysorbate 20INACTIVE INGREDIENT7T1F30V5YH1
WaterINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51870-00151870-001-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
HYDROXYETHYL CELLULOSE, UNSPECIFIEDT4V6TWG28DIACT
GLYCERINPDC6A3C0OXIACT
POLYSORBATE 207T1F30V5YHIACT
EDETATE SODIUMMP1J8420LUIACT
ALUMINUM CHLOROHYDRATEHPN8MZW13MACTIB

Source Document#

Source XML · Source PDF

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
132024-11-15full-release2026-06-01 00:37:30

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 · 8 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
Polysorbate 20POLYSORBATE 207T1F30V5YHSOLUTION / TOPICAL15 %w/wExact identifier — unii+route+dosage form
2 equally ranked IID candidates
Edetate SodiumEDETATE SODIUMMP1J8420LUSOLUTION / TOPICAL0.3 %w/wExact identifier — unii+route+dosage form
2 equally ranked IID candidates
GlycerinGLYCERINPDC6A3C0OXSOLUTION / TOPICAL1971 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%)HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%)S38J6RZN16SOLUTION / TOPICAL0.21 %w/vExact identifier — unii+route+dosage form
2 equally ranked IID candidates
GlycerinGLYCERINPDC6A3C0OXSOLUTION / TOPICAL1971 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
Edetate SodiumEDETATE SODIUMMP1J8420LUSOLUTION / TOPICAL0.3 %w/wExact identifier — unii+route+dosage form
2 equally ranked IID candidates
Polysorbate 20POLYSORBATE 207T1F30V5YHSOLUTION / TOPICAL15 %w/wExact identifier — unii+route+dosage form
2 equally ranked IID candidates
HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%)HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%)S38J6RZN16SOLUTION / TOPICAL0.21 %w/vExact identifier — unii+route+dosage form
2 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
Roll On Anti-Perspirant DeodorantALUMINUM CHLOROHYDRATEKeefe Group9a1bd5aa-8720-42fe-a157-d06d122a893c2026-01-08WarningsExact identifier
ndc (package): 51870-001-03
ndc (product): 51870-001
ndc11 (package): 51870000103
spl id: 47e5f195-d2d1-cacd-e063-6394a90a2adf
spl set id: 9a1bd5aa-8720-42fe-a157-d06d122a893c

Reported adverse events (FAERS/openFDA)#

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