FDA.reportPublic FDA data

Palmero Healthcare Discide XRA Hand Sanitizing Wipes

Manufacturer
Palmero Healthcare, LLC
Effective date
2025-12-04
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
monthly-update
Hydrated at
2026-06-03 17:45:24

Label at a glance#

ProductPalmero Healthcare Discide XRA Hand Sanitizing Wipes
Active ingredientALCOHOL
Label structure7 sections

Indications and uses

For handwashing to decrease bacteria on the skin.  After changing diapers.  After assisting ill persons.  Before contact with a person under medical care or treatment.

Dosage and administration

Wet hands thoroughly with product and allow to dry.  Children under six years of age should be supervised when using this product.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • For handwashing to decrease bacteria on the skin. 
  • After changing diapers. 
  • After assisting ill persons. 
  • Before contact with a person under medical care or treatment.

Warnings

WARNINGS SECTION

Flammable. Keep away from fire or flame.

For external use only.

Do not use

OTC - DO NOT USE SECTION

in the eyes.

When using this product

OTC - WHEN USING SECTION

do not get into eyes. If contact occurs, rinse thoroughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation and redness develop. If condition persists for more than 72 hours consult a doctor.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Wet hands thoroughly with product and allow to dry. 
  • Children under six years of age should be supervised when using this product.

Other information

SPL UNCLASSIFIED SECTION

  • Store below 110°F (43°C).

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Propylene Glycol, Undeceth-7, Isopropyl Myristate, Aloe Barbadensis Leaf Juice, Methyl Salicylate, Tocopheryl Acetate (Vitamin E).

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BottleBottle

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130840415100021GTIN-13: 0840415100021
EAN-13: 0840415100021
GTIN-12: 840415100021
UPC-A: 840415100021
GTIN storage (14 digits): 00840415100021		Bottle.jpg

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74545-00274545-002-16

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
UNDECETH-7R6B5PCO2JNIACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
ALOE VERA LEAFZY81Z83H0XIACT
METHYL SALICYLATELAV5U5022YIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
ALCOHOL3K9958V90MACTIB

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
4527893c-d7d9-e83e-e063-6394a90afae3b3c46b92-3d0c-d6c2-e053-2995a90ab7c32025-12-04WarningsExact identifier
spl id: 4527893c-d7d9-e83e-e063-6394a90afae3
spl set id: b3c46b92-3d0c-d6c2-e053-2995a90ab7c3

Reported adverse events (FAERS/openFDA)#

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