FDA.reportPublic FDA data

XERO Antiperspirant Wipe

Manufacturer
Stock Your Home | Diamond Wipes International, Inc
Effective date
2026-08-05
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
daily-update
Hydrated at
2026-08-08 02:01:10

Label at a glance#

ProductAntiperspirant Wipe
Active ingredientALUMINUM CHLOROHYDRATE
Label structure8 sections

Dosage and administration

■ open packet ■ remove and unfold wipe ■ apply to underarm only

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum Chlorohydrate 15%

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Use

INDICATIONS & USAGE SECTION

Reduces underarm perspiration

Warnings

WARNINGS SECTION

For external use only

Do not use

■ on broken or irritation skin

■ immediately after shaving

Ask a doctor before use if you have kidney disease

When using this product ■ do not use in or near eyes ■ apply to underarms only

Stop use and ask a doctor if rash or irritation develops

Keep out of reach of children

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.

Directions

DOSAGE & ADMINISTRATION SECTION

■ open packet ■ remove and unfold wipe ■ apply to underarm only

Inactive ingredients

INACTIVE INGREDIENT SECTION

benzoic acid, benzyl alcohol, chlorphenesin, fragrance, PEG-180, phenoxyethanol, polysorbate 20, potassium sorbate, salvia officinalis (sage) leaf extract, sorbic acid, tocopherol, tocopheryl acetate, usnea barbata (lichen) extract, water

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

XERO

ANTIPERSPIRANT WIPES

ALL DAY SWEAT & ODOR

PROTECTION

24- HOER PROTECTION

DO NOT FLUSH

1 WIPE

LABELLABEL

10 WIPES

LABELLABEL

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717
9869efd7-d6dd-0665-5b67-53adbe6ef15eProduct name120140508

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
85505-39585505-395-01

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
ALUMINUM CHLOROHYDRATEHPN8MZW13MACTIB
POLYSORBATE 207T1F30V5YHIACT
PHENOXYETHANOLHIE492ZZ3TIACT
WATER059QF0KO0RIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
TOCOPHEROLR0ZB2556P8IACT
USNEA BARBATAD6DVA9TCAPIACT
SORBIC ACIDX045WJ989BIACT
CHLORPHENESINI670DAL4SZIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
SAGE065C5D077JIACT
BENZOIC ACID8SKN0B0MIMIACT
BENZYL ALCOHOLLKG8494WBHIACT
PEG-180Q662QK8M3BIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22025-04-22full-release2026-06-01 00:59:54

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
Antiperspirant WipeALUMINUM CHLOROHYDRATEStock Your Home326c944a-8beb-d33d-e063-6294a90ae2a92026-08-05WarningsExact identifier
ndc (package): 85505-395-01
ndc (product): 85505-395
ndc11 (package): 85505039501
spl id: 584dffd9-059e-ee73-e063-6394a90ad62d
spl set id: 326c944a-8beb-d33d-e063-6294a90ae2a9

Reported adverse events (FAERS/openFDA)#

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