Hand Sanitizer

Manufacturer
Pluma Nacional S.a. de C.V.
Effective date
2022-06-29
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:57:52

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

For hand sanitizing to decrease bacteria on the skin. Recommended for repeated use.

Dosage and administration

Not recommended for infants. Wet hands thoroughly with product and allow to dry without wiping. Children under 6 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 hand sanitizing to decrease bacteria on the skin. Recommended for repeated use.

WARNINGS

WARNINGS SECTION

Flammable. Keep away from fire or flame. For external use only hands.

Avoid contact with broken skin.

When using this product

OTC - WHEN USING SECTION

do not use in or near eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation or rash appears and lasts.

KEEP OUT OF REACH OF CHILDREN.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Not recommended for infants. Wet hands thoroughly with product and allow to dry without wiping. Children under 6 years of age should be supervised when using this product.

OTHER INFORMATION

SPL UNCLASSIFIED SECTION

Do not store above 30°C.  may discolor fabrics.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Aqua(water), Glycerin, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, triethanolamine, Aloe Barbadensis Leaf Extract, Parfum(Fragrance)water.

Package Labeling:30ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle3Bottle3Bottle4Bottle4

Package Labeling:60ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle5Bottle5Bottle6Bottle6

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
52381-00252381-002-01, 52381-002-02

Ingredients#

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

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

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
e295c540-5a1d-64d3-e053-2995a90ab2f9b0796582-d52e-6985-e053-2a95a90ad8632022-06-29WarningsExact identifier
spl id: e295c540-5a1d-64d3-e053-2995a90ab2f9
spl set id: b0796582-d52e-6985-e053-2a95a90ad863

Reported adverse events (FAERS/openFDA)#

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