FDA.reportPublic FDA data

PURE DASH Antiseptic Hand ALMOND SCENTED

Manufacturer
Prime Lab, LLC
Effective date
2023-10-28
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:23:02

Label at a glance#

ProductPURE DASH Antiseptic Hand ALMOND SCENTED
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections

Dosage and administration

Wet hands and forearms. Apply 5 milliliters (teaspoonful) or palmful to hands and forearms.scrub thoroughly for at least 30 seconds. Rinse and repeat.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.13%

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 5 milliliters (teaspoonful) or palmful to hands and forearms.scrub thoroughly for at least 30 seconds. Rinse and repeat.

Other information

SPL UNCLASSIFIED SECTION

  • Protect from freezing
  • Keep tightly closed in a dry, cool, and well-ventilated place

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, sodium lauryl sulfate, coco betaine, coconut diethanolamide, sodium chloride, fragrance, citric acid

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79937-01179937-011-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
SODIUM LAURYL SULFATE368GB5141JIACT
COCO-BETAINE03DH2IZ3FYIACT
COCO DIETHANOLAMIDE92005F972DIACT
SODIUM CHLORIDE451W47IQ8XIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
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
0fb28392-af4d-9c25-e063-6294a90ace1657306843-6b27-41b1-992d-ab19abc31f2c2024-01-24WarningsExact identifier
spl set id: 57306843-6b27-41b1-992d-ab19abc31f2c

Reported adverse events (FAERS/openFDA)#

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