FDA.reportPublic FDA data

Waltz Free Hand Sanitizer Foam

Manufacturer
AvKARE
Effective date
2021-01-26
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 22:54:37

Label at a glance#

ProductWaltz Free Hand Sanitizer Foam
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Indications and uses

For hand sanitizing. To decrease bacteria on the skin.

Dosage and administration

Apply a small amount on your hands. Rub hands together until dry. When hands are visibly soiled, wash with soap and water. Store in cool, dry area.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

DRUG FACTS

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

For hand sanitizing. To decrease bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only.

Do not use in the eyes.

OTC - DO NOT USE SECTION

In case of eye contact, rinse eyes thoroughly with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation or redness develops or if condition persists more than 72 hours.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Instruct children on proper use. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply a small amount on your hands. Rub hands together until dry. When hands are visibly soiled, wash with soap and water. Store in cool, dry area.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Extract, Avena Sativa (Oat) Extract, Behentrimonium Methosulfate, Butylene Glycol, Caprylyl Glycol, Centrimonium Chloride, Dimethicone, Emulsifying Wax NF, Glycerin, Hydrolyzed Soy Protein, Mentha Piperita (Peppermint) Essential Oil, Phenoxyethanol, Retinyl Palmitate Vitamin A, Simmondsia Chinensis (Jojoba) Seed Oil, Sorbic Acid, Tetrasodium EDTA, Tocopheryl Acetate Vitamin E, Water

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1.71.7

27oz27oz

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
73190-002-02ML - Milliliter73190-002b9fe5188-4caf-490a-b8cd-9ca4fb7b2bc312019-10-07
73190-002-27ML - Milliliter73190-002dbda2888-f9c5-4a9c-a842-3157bee5d1ab12019-10-07

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73190-00273190-002-02, 73190-002-27

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ALOE VERA LEAFZY81Z83H0XIACT
GLYCERINPDC6A3C0OXIACT
CITRUS MAXIMA SEED083X55C543IACT
THYMECW657OBU4NIACT
GREEN TEA LEAFW2ZU1RY8B0IACT
AVENA SATIVA LEAF206PI19V7RIACT
PEPPERMINT OILAV092KU4JHIACT
POLYSORBATE 207T1F30V5YHIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
SODIUM BENZOATEOJ245FE5EUIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

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
f15fff64-2320-62c6-e053-2995a90ad912903d337f-4949-398f-e053-2a95a90a866e2023-01-03WarningsExact identifier
spl set id: 903d337f-4949-398f-e053-2a95a90a866e

Reported adverse events (FAERS/openFDA)#

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