Germ Bloc Hand Sanitizer Foam Peppermint

Manufacturer
AvPAK
Effective date
2020-01-20
Label type
HUMAN OTC DRUG LABEL
Version
10
Source
legacy-cache
Hydrated at
2026-08-01 23:45:12

Label at a glance#

ProductGerm Bloc Hand Sanitizer Foam Peppermint
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

Water, Aloe Barbadensis Leaf Extract, Glycerin, Citrus Grandis (Grapefruit) Seed Extract, Thymus Vulgaris (Thyme) Extract, Camellia Sinensis Leaf (Green Tea) Extract, Avena Sativa (Oat) Extract, Peppermint Essential Oil, Polysorbate 20, Potassium Sorbate, Sodium Benzoate.

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Alcohol-Free Formula
GERM BLOCTM
Kills 99.99% of Germs
Hand Sanitizer
Foam      
10 fl. oz. / 300 ml

1
1

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50268-354-08ML - Milliliter50268-354738a77d3-8822-4818-8e5e-bffdf8b86ee912018-03-08
50268-354-10ML - Milliliter50268-3543333b928-73bd-43f3-a01e-e5201a4aa05c12018-03-08

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
50268-35450268-354-02, 50268-354-08, 50268-354-10, 50268-354-27, 50268-354-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 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
d5dd5964-28dd-a14c-e053-2a95a90af15a9f8c8d26-c600-707c-67a1-b031bb4e0c9b2022-01-18WarningsExact identifier
spl set id: 9f8c8d26-c600-707c-67a1-b031bb4e0c9b

Reported adverse events (FAERS/openFDA)#

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