Foaming Hand Sanitizer Refill Moisturizing Aloe

Manufacturer: Bocks Inc
Effective date: 2021-02-08
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:37:54

Label at a glance#

ProductFoaming Hand Sanitizer Refill Moisturizing Aloe

Active ingredientBENZALKONIUM CHLORIDE

Label structure7 sections

Indications and uses

• hand sanitizer that helps decrease bacteria on the skin • recommend for repeated use

Dosage and administration

• pour liquid into a foaming dispenser • pump a small amount of foam into palm of hand • spread thoroughly on both hands • rub hands together until dry

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

• hand sanitizer that helps decrease bacteria on the skin
• recommend for repeated use

Warnings

WARNINGS SECTION

For external use only, do not use in ears, mouth, or eyes.

When using this product

OTC - WHEN USING SECTION

avoid contact with eyes. In case of eye contact, flush eyes with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

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

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Children should be supervised when using this product.

Directions

DOSAGE & ADMINISTRATION SECTION

• pour liquid into a foaming dispenser
• pump a small amount of foam into palm of hand
• spread thoroughly on both hands
• rub hands together until dry

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aloe Juice, Citric Acid, Dimonium Chloride Cocoamidopropyl Hydroxyethyldimonium Chloride, Hydroxypropyl Bis-Hydroxyethyldimonium Chloride,Rose Ether, Sodium Citrate, Water

Package Labeling: 473ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle3

Package Labeling: 946ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle4

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1020365	benzalkonium chloride 0.13 % Topical Foam	PSN	1
1020365	benzalkonium chloride 1.3 MG/ML Topical Foam	SCD	1
1020365	benzalkonium chloride 0.13 % Topical Foam	SY	1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
d5e51f11-ad28-caa4-4b49-4143974782ad	Product name	1	20150831

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
81527-001-16	2023-01-30	C162847	48780-1	f386c649-a365-0266-e053-dadaa90a7c1a	Foaming Hand Sanitizer Refill (Moisturizing Aloe)
81527-001-32	2023-01-30	C162847	48780-1	f386c649-a365-0266-e053-dadaa90a7c1a	Foaming Hand Sanitizer Refill (Moisturizing Aloe)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
81527-001-16	Foaming Hand Sanitizer Refill Moisturizing Aloe	473 mL in 1 CARTON	LIQUID	473		1
81527-001-32	Foaming Hand Sanitizer Refill Moisturizing Aloe	946 mL in 1 CARTON	LIQUID	946		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
81527-001	FOAMING HAND SANITIZER REFILL MOISTURIZING ALOE (BENZALKONIUM CHLORIDE) LIQUID [BOCKS INC]	1	Legacy NDC, 2 package rows	20210209_18e15a27-b6ce-4bfa-933c-405e8011639d.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

Foaming Hand Sanitizer Refill Moisturizing Aloe
BENZALKONIUM CHLORIDE
ALOE VERA LEAF
CITRIC ACID MONOHYDRATE
HYDROXYPROPYL BIS-HYDROXYETHYLDIMONIUM CHLORIDE
SODIUM CITRATE
WATER
BENZALKONIUM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
81527-001	81527-001-16, 81527-001-32

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALOE VERA LEAF	ZY81Z83H0X	IACT
CITRIC ACID MONOHYDRATE	2968PHW8QP	IACT
HYDROXYPROPYL BIS-HYDROXYETHYLDIMONIUM CHLORIDE	1EO3O1X7HG	IACT
SODIUM CITRATE	1Q73Q2JULR	IACT
WATER	059QF0KO0R	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
bad1ce99-8df1-def4-e053-2995a90a5622			18e15a27-b6ce-4bfa-933c-405e8011639d	2021-02-08	Warnings	Exact identifier spl id: bad1ce99-8df1-def4-e053-2995a90a5622 spl set id: 18e15a27-b6ce-4bfa-933c-405e8011639d

Reported adverse events (FAERS/openFDA)#

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