FDA.reportPublic FDA data

Dr Pure Antiseptic Liquid Hand Apple and Cucumber Scented

Manufacturer
Industrias Bernal Canton S.A. de C.V.
Effective date
2023-03-21
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:34:13

Label at a glance#

ProductDr Pure Antiseptic Liquid Hand Apple and Cucumber Scented
Active ingredientBENZALKONIUM CHLORIDE
Label structure6 sections

Dosage and administration

Wet hands and forearms. Apply palmful to hands and forearms. Scrub thoroughly. Rinse and repeat

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.1%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

For hand washing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

in the eyes.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • irritation and redness develop
  • 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.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Wet hands and forearms.
  • Apply palmful to hands and forearms.
  • Scrub thoroughly.
  • Rinse and repeat

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Sodium Lauryl Sulfate, Sodium Chloride, Cocamidopropyl Betaine, DMDM Hydantoin, Glycerol, Cucumis Sativus Extract, Aloe Barbadensis Leaf Juice Extract, Fragrance, Color Yellow No. 5 (Cl 19140) and Blue No 1 (CI 42090).

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2Label2

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
78239-00478239-004-16

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
SODIUM LAURETH SULFATEBPV390UAP0IACT
SODIUM CHLORIDE451W47IQ8XIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
DMDM HYDANTOINBYR0546TOWIACT
GLYCERINPDC6A3C0OXIACT
ALOE VERA LEAFZY81Z83H0XIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

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
f76d6c3e-241d-ded4-e053-6294a90af58cc4f81f56-2b88-1d22-e053-2995a90a5bbd2023-03-21WarningsExact identifier
spl id: f76d6c3e-241d-ded4-e053-6294a90af58c
spl set id: c4f81f56-2b88-1d22-e053-2995a90a5bbd

Reported adverse events (FAERS/openFDA)#

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