FDA.reportPublic FDA data

United Spirit of America

Manufacturer
Prime Enterprises, Inc.
Effective date
2023-08-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:27:38

Label at a glance#

ProductUnited Spirit of America Anti Perspirant Deodorant
Active ingredientALUMINUM CHLOROHYDRATE
Label structure7 sections

Indications and uses

Decreases underarm perspiration.

Dosage and administration

Directions Apply to underarms only

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Aluminum Chlorohydrate 25%

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Uses

INDICATIONS & USAGE SECTION

Decreases underarm perspiration.

Warnings

WARNINGS SECTION

For external use only.

OTC - DO NOT USE SECTION

Do not useon broken skin.

OTC - STOP USE SECTION

Stop useif rash or irritation occurs.

OTC - ASK DOCTOR SECTION

Ask a doctor before useif you havekidney 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.

Other Information

SPL UNCLASSIFIED SECTION

Other InformationDo not store above 115°F.

Directions

DOSAGE & ADMINISTRATION SECTION

DirectionsApply to underarms only

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, SD Alcohol 40-B, Cyclopentasiloxane, Glycerin, Glyceryl Stearate, PEG-100 Stearate, Cyclohexasiloxane, Cetyl Alcohol, Phenoxyethanol, Ethylhexylglycerin, Fragrance, Magnesium Aluminum Silicate, Tetrasodium EDTA, Xanthan Gum

Warrior Nano Shield Deodorant Anti-Perspirant Roll On

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Principal Display LabelPrincipal Display Label

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
58443-063558443-0635-3

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
NameUNIIKind
PHENOXYETHANOLHIE492ZZ3TIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
CETYL ALCOHOL936JST6JCNIACT
CYCLOMETHICONE 6XHK3U310BAIACT
XANTHAN GUMTTV12P4NEEIACT
EDETATE SODIUM TETRAHYDRATEL13NHD21X6IACT
GLYCERYL STEARATE SEFCZ5MH785IIACT
PEG-100 STEARATEYD01N1999RIACT
GLYCERINPDC6A3C0OXIACT
ALCOHOL3K9958V90MIACT
CYCLOMETHICONE 50THT5PCI0RIACT
MAGNESIUM ALUMINUM SILICATE6M3P64V0NCIACT
WATER059QF0KO0RIACT
ALUMINUM CHLOROHYDRATEHPN8MZW13MACTIB

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
021b55c0-e2ac-21c5-e063-6394a90a29ef021b4c50-a98b-5a3c-e063-6394a90abebb2023-08-04WarningsExact identifier
spl id: 021b55c0-e2ac-21c5-e063-6394a90a29ef
spl set id: 021b4c50-a98b-5a3c-e063-6394a90abebb

Reported adverse events (FAERS/openFDA)#

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