Active Ingredient

Manufacturer
Twin Med LLC
Effective date
2026-05-29
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
daily-update
Hydrated at
2026-06-03 18:03:29

Label at a glance#

ProductProCure Foaming Hand Sanitizer
Active ingredientALCOHOL
Label structure7 sections

Indications and uses

Uses hand sanitizer to help reduce bacteria on the skin that could cause disease

Dosage and administration

Directions Put enough product on your palm to cover hands and rub hands together bristly until dry 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 72% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

Uses hand sanitizer to help reduce bacteria on the skin that could cause disease

Warnings

WARNINGS SECTION

Warnings

For external use only

FLAMMABLE. Keep away from fire or flame

When using this product

OTC - WHEN USING SECTION

When using this product

  • do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water
  • avoid contact with broken skin
  • do not inhale or ingest

Stop use and ask a doctor if

OTC - STOP USE SECTION

Stop use and ask a doctor if

  • irritation or redness develops
  • condition persists for more than 72 hours

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

Directions

  • Put enough product on your palm to cover hands and rub hands together bristly until dry
  • Children under 6 years of age should be supervised when using this product

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Inactive Ingredients Aloe Barbadensis Leaf Juice, Disodium EDTA, Glycerin, Isopropyl Myristate, PEG-10 Dimethicone, Polyquaternium-11, Tocopheryl Acetate, Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Hand Sanitizer FOAMHand Sanitizer FOAM

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2277550ethanol 72 % Topical GelPSN2
2277550ethanol 0.72 ML/ML Topical GelSCD2
2277550ethanol 72 % Topical GelSY2

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeCode 128(01)10840330706473GTIN-14: 10840330706473
GTIN storage (14 digits): 10840330706473
HAND SANITIZER 1000mL FOAMpdf.jpg

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55681-04055681-040-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12025-08-29full-release2026-06-01 01:12:15

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
ProCure Foaming Hand SanitizerETHYL ALCOHOL 72%Twin Med LLC3d848ec8-5197-6d39-e063-6394a90aaef62026-05-29WarningsExact identifier
ndc (package): 55681-040-10
ndc (product): 55681-040
ndc11 (package): 55681004010
spl id: 52f7e8b4-f263-b053-e063-6394a90ae47a
spl set id: 3d848ec8-5197-6d39-e063-6394a90aaef6

Reported adverse events (FAERS/openFDA)#

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