PH Simply Hand and Skin Sanitizer

Manufacturer
Paris Honore, LLC
Effective date
2022-01-13
Label type
HUMAN OTC DRUG LABEL
Version
11
Source
legacy-cache
Hydrated at
2026-08-01 22:17:03

Label at a glance#

ProductOne Complete Microbarrier
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Indications and uses

For hand and skin sanitizing to decrease microbes on skin Recommended for repeated use

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient Purpose

Benzalkonium Chloride 0.1%..................................Antimicrobial

Uses

OTC - PURPOSE SECTION

For hand and skin sanitizing to decrease microbes on skin
Recommended for repeated use

INSTRUCTIONS FOR USE SECTION

Apply a small amount to hands or skin.
Rub thoroughly over surfaces. Rub briskly until dry.

Warnings

WARNINGS SECTION

For external use only.

When using this product avoid contact with eyes. In case of eye contact, flush eyes with water.

OTC - WHEN USING SECTION

When using this product avoid contact with eyes. In case of eye contact, flush eyes with water.

OTC - ASK DOCTOR SECTION

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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

OTC - STOP USE SECTION

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

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Polysilsesquioxane Steardimonium Chloride

PH Simply Hand & Skin Sanitiser

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Drug Facts

Active ingredient Purpose

Benzalkonium Chloride 0.13%..................................Antimicrobial

Uses

•For hand and skin sanitizing
•Recommended for repeated use

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.

Directions

•Apply a small amount to hands or skin.
•Rub thoroughly over surfaces. Rub briskly until dry.

Inactive ingredients Water, Polysilsesquioxane Steardimonium Chloride, fragrance

Package LabelPackage Label

FDA-Initiated Inactive NDC Indexing#

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71370-70071370-700-10, 71370-700-80, 71370-700-22, 71370-700-55, 71370-700-50, 71370-700-60, 71370-700-99

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 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
e78ce1f8-4683-8fd1-e053-2a95a90a77914be52dfe-2f0d-71b3-e054-00144ff8d46c2022-08-31WarningsExact identifier
spl set id: 4be52dfe-2f0d-71b3-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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