PureCareRx Foaming Hand Sanitizer

Manufacturer
Purechempros LLC
Effective date
2023-01-10
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:41:12

Label at a glance#

ProductPureCareRx Foaming Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient .................................................Purpose
Benzalkonium Chloride 0.1%..............................Antimicrobial

Active Ingredient SectionActive Ingredient Section

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.

Keep Out of Reach of ChildrenKeep Out of Reach of Children

OTC - PURPOSE SECTION

Purpose SectionPurpose Section

OTC - ASK DOCTOR SECTION

Stop use and ask a doctor if irritation or redness
develops, or if condition persists for more than 72 hours.

Stop use and ask a doctorStop use and ask a doctor

OTC - WHEN USING SECTION

When using this productWhen using this productavoid contact with eyes.
In case of eye contact, flush eyes with water.

DOSAGE & ADMINISTRATION SECTION

Pump a small amount of foam into palm of hand

Rub thoroughly over all surfaces of both hands

Rub hands together briskly until dry

WARNINGS SECTION

Warnings
For external use only

When using this product avoid contact with eyes. In case of
eye contact, flush eyes with water.
Stop use and ask a doctor if irritation or redness develops,
or if condition persists for more than 72 hours.
Keep out of reach of children. If swallowed, get medical
help or contact a Poison Control Center right away.

INACTIVE INGREDIENT SECTION

Inactive ingredients Water, cetrimonium chloride,
laurtrimonium chloride, dihydroxyethyl cocamine oxide,
glycereth-17 cocoate, citric acid, fragrance

INDICATIONS & USAGE SECTION

Uses

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Principal Display PanelPrincipal Display Panel3785.41mL NDC: 31511-007

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81966-00181966-001-01

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
04b2fab6-3660-51d6-e063-6294a90ae78cc32fb66d-b2c3-904b-e053-2995a90aa2682023-09-06WarningsExact identifier
spl set id: c32fb66d-b2c3-904b-e053-2995a90aa268

Reported adverse events (FAERS/openFDA)#

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