Germ Bloc Hand Sanitizer Lotion

Manufacturer
AvPAK
Effective date
2020-01-20
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
legacy-cache
Hydrated at
2026-08-01 23:45:15

Label at a glance#

ProductGerm Bloc Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Indications and uses

Kills 99.99 % germs and moisturizes skin.

Dosage and administration

Apply a small amount to hands every 3 to 4 hours and rub until dry. Does not replace soap and water. 

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

Kills 99.99 % germs and moisturizes 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 to hands every 3 to 4 hours and rub until dry. Does not replace soap and water. 

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

ALCOHOL-FREE
Kills 99.99% of Germs
GERM BLOCTM 
Hand
Sanitizer
Lotion
8 fl. oz. (237 ml)

label
label

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50268-353-01ML - Milliliter50268-35350fe7f8a-63ba-45a9-8ea6-1b82047fae8112017-11-06
50268-353-02ML - Milliliter50268-35387f07a35-aa4b-4009-bcd0-f9a7ad9ff23912017-10-13
50268-353-08ML - Milliliter50268-35307c66f41-e7c6-4ce1-ab04-47ffba73591512017-09-11
50268-353-16ML - Milliliter50268-35356af36d2-86a8-466e-8d30-4343615cc23c12017-09-11
50268-353-27ML - Milliliter50268-353ce457383-228d-4b97-92b7-94fa7b954ee112017-09-11
50268-353-32ML - Milliliter50268-35394751575-a186-4440-9118-0714e866d84112017-09-11

Products#

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

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
50268-35350268-353-08, 50268-353-16, 50268-353-32, 50268-353-02, 50268-353-27, 50268-353-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 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
d5dd6353-8f47-1001-e053-2995a90ab3b4c04141ed-e6c7-6549-33d8-57abf70f9e492022-01-18WarningsExact identifier
spl set id: c04141ed-e6c7-6549-33d8-57abf70f9e49

Reported adverse events (FAERS/openFDA)#

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