Natural Concepts Non-Alcohol Foaming Hand Sanitizer

Manufacturer: Apollo Health and Beauty Care Inc.
Effective date: 2020-07-17
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:21:51

Label at a glance#

ProductNatural Concepts Non-Alcohol Foaming Hand Sanitizer

Active ingredientBENZALKONIUM CHLORIDE

Label structure8 sections

Indications and uses

to help decrease bacteria on the skin. For use when soap and water are not available.

Dosage and administration

Pump enough product to your palm to thoroughly cover your hands, rub together for at least 30 seconds, until dry. Children under 6 years should be supervised when using this product.

Storage and handling

store at room temperature.

Contacts and useful links#

PhoneLabel contact1-866-695-3030

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

to help decrease bacteria on the skin. For use when soap and water are not available.

Warnings

WARNINGS SECTION

For external use only.

When using this product

OTC - WHEN USING SECTION

avoid contact with eyes. If contact occurs, rinse thoroughly with water.

Do not use

OTC - DO NOT USE SECTION

on children less than 2 months of age
on open wounds

Stop useing this product and ask a doctor if

OTC - STOP USE SECTION

irritation or redness develops and lasts more than 7 days.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, get medical help or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Pump enough product to your palm to thoroughly cover your hands, rub together for at least 30 seconds, until dry.
Children under 6 years should be supervised when using this product.

Other information

STORAGE AND HANDLING SECTION

store at room temperature.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Polysorbate 20, PPG-26-Buteth-26, PEG-40 Hydrogenated Castor Oil, Aloe Barbadensis Leaf Juice, Fragrance (Parfum), Camellia Sinensis Leaf Extract, DMDM Hydantoin, Sodium Hydroxide, Blue 1 (CI 42090), Yellow 5 (CI 19140)

Questions or comments?

OTC - QUESTIONS SECTION

1-866-695-3030

Label copy

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of the label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1038799	benzalkonium chloride 0.1 % Topical Foam	PSN	1
1038799	benzalkonium chloride 1 MG/ML Topical Foam	SCD	1
1038799	benzalkonium chloride 0.1 % Topical Foam	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
63148-513-37	2024-01-30	C162847	48780-1	1030e365-033c-111a-e063-dadaa90a10e2	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
63148-513-37	Natural Concepts Non-Alcohol Foaming Hand Sanitizer	3785 mL in 1 BOTTLE, PLASTIC	SOLUTION	3785		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
63148-513	NATURAL CONCEPTS NON-ALCOHOL FOAMING HAND SANITIZER (BENZALKONIUM CHLORIDE) SOLUTION [APOLLO HEALTH AND BEAUTY CARE INC.]	1	Legacy NDC, 1 package rows	20200718_d252b7fb-cd0b-4600-8acc-e4d8dd5724fa.zip

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

Natural Concepts Non-Alcohol Foaming Hand Sanitizer
Benzalkonium Chloride
BENZALKONIUM
WATER
POLYSORBATE 20
PPG-26-BUTETH-26
POLYOXYL 40 HYDROGENATED CASTOR OIL
ALOE VERA LEAF
GREEN TEA LEAF
DMDM HYDANTOIN
FD&C BLUE NO. 1
FD&C YELLOW NO. 5
SODIUM HYDROXIDE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
63148-513	63148-513-37

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB
WATER	059QF0KO0R	IACT
POLYSORBATE 20	7T1F30V5YH	IACT
PPG-26-BUTETH-26	2II1K6TZ4P	IACT
POLYOXYL 40 HYDROGENATED CASTOR OIL	7YC686GQ8F	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
GREEN TEA LEAF	W2ZU1RY8B0	IACT
DMDM HYDANTOIN	BYR0546TOW	IACT
FD&C BLUE NO. 1	H3R47K3TBD	IACT
FD&C YELLOW NO. 5	I753WB2F1M	IACT
SODIUM HYDROXIDE	55X04QC32I	IACT

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
04d1b244-604d-4339-8abc-0ba8f51088b5			d252b7fb-cd0b-4600-8acc-e4d8dd5724fa	2020-07-17	Warnings	Exact identifier spl id: 04d1b244-604d-4339-8abc-0ba8f51088b5 spl set id: d252b7fb-cd0b-4600-8acc-e4d8dd5724fa

Reported adverse events (FAERS/openFDA)#

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