FDA.reportPublic FDA data

Juniper Breeze Foaming Antimicrobial

Manufacturer
Hillyard GMP
Effective date
2023-12-04
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:19:18

Label at a glance#

ProductJuniper Breeze Foaming Antimicrobial
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Indications and uses

• Helps reduce bacteria that potentially can cause disease • Helps prevent cross-contamination by hand contact

Dosage and administration

• Apply soap to palm of hand. • Lather and scrub hands (including fingers, wrist, and cuticles) vigorously for 60 seconds. • Rinse with water until all soap is removed from hands. • Dry completely (incomplete drying may lead to chapped skin). • Children under 6 years of age should be supervised when using this product.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

  • Helps reduce bacteria that potentially can cause disease
  • Helps prevent cross-contamination by hand contact

Warnings

WARNINGS SECTION

  • For External Use Only
  • Do not contaminate water, food or feed by storage and disposal.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • In case of eye contact, flush with water for 15 minutes. If irritation persists, get medical attention. In case of accidental ingestion, seek medical attention or contact a poison control center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Apply soap to palm of hand.
  • Lather and scrub hands (including fingers, wrist, and cuticles) vigorously for 60 seconds.
  • Rinse with water until all soap is removed from hands.
  • Dry completely (incomplete drying may lead to chapped skin).
  • Children under 6 years of age should be supervised when using this product.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Cocamidopropylamine Oxide, Glycerin, Propanediol, Benzyl Alcohol, Phenoxyethanol, Cetrimonium Chloride, Fragrance, Laurtrimonium Chloride, Dihydroxyethyl Cocamine Oxide, Glycereth-17 Cocoate, Yellow #6, Aloe Barbadensis Leaf Juice, Citric Acid.

Principal Display Panel – 1 Liter

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Hillyard

Juniper Breeze Foaming Antimicrobial Hand Soap

HIL0040502

affinity
TOUCH-FREE

Place cartridge into dispenser, label facing back, and gently push pump into receiver until it clicks into place.

To remove the cartridge and pump, rotate the green ring clockwise and pull the pump out.

HILLYARD INDUSTRIES, INC.
PO Box 909
St. Joseph, MO
64502-0909
Telephone: 816-233-1321
www.hillyard.com

NET CONTENTS 33.8 FL OZ OR 1 L
PEEL HERE

image-01
image-01

Label

Principal Display Panel – 1.25 Liter

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Hillyard

Juniper Breeze Foaming Antimicrobial Hand Soap

HIL0040503

affinity
DISPENSING SYSTEM

Place cartridge into dispenser, label facing back, and gently push pump into receiver until it clicks into place.

To remove the cartridge and pump, rotate the green ring clockwise and pull the pump out.

HILLYARD INDUSTRIES, INC.
PO Box 909
St. Joseph, MO
64502-0909
Telephone: 816-233-1321
www.hillyard.com

NET CONTENTS 42.3 FL OZ OR 1.25 L
PEEL HERE

image-02
image-02

Label

Principal Display Panel – 1 US Gallon

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Hillyard

Juniper Breeze Foaming Antimicrobial Hand Soap
An Antimicrobial, Triclosan-Free Hand Soap To Decrease Bacteria On The Skin

HIL0040506

CAUTION
KEEP OUT OF REACH OF CHILDREN
(See back panels for additional precautions)

HILLYARD
Hand & BODY CARE

HILLYARD INDUSTRIES, INC. • PO Box 909 • St. Joseph, Missouri 64502-0909 • Telephone: 816-233-1321 • www.hillyard.com

NET CONTENTS: 1 US GAL OR 3.785 LITERS

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image-03

Label

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76402-40576402-405-02, 76402-405-03, 76402-405-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT
COCAMIDOPROPYLAMINE OXIDEM4SL82J7HKIACT
GLYCERINPDC6A3C0OXIACT
PROPANEDIOL5965N8W85TIACT
BENZYL ALCOHOLLKG8494WBHIACT
PHENOXYETHANOLHIE492ZZ3TIACT
CETRIMONIUM CHLORIDEUC9PE95IBPIACT
LAURTRIMONIUM CHLORIDEA81MSI0FICIACT
DIHYDROXYETHYL COCAMINE OXIDE8AR51R3BL5IACT
GLYCERETH-17 COCOATE3057VPT0KCIACT
ALOE VERA LEAFZY81Z83H0XIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT

Source Document#

Source XML · Source PDF

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
f3e3768b-7cc8-400a-be77-49867b2058fb43002f20-6d4d-42b3-945d-c0a69d9c40912023-12-04WarningsExact identifier
spl id: f3e3768b-7cc8-400a-be77-49867b2058fb
spl set id: 43002f20-6d4d-42b3-945d-c0a69d9c4091

Reported adverse events (FAERS/openFDA)#

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