P.O.V. Antibacterial Foaming Hand

Manufacturer: Apollo Health and Beauty Care Inc.
Effective date: 2017-11-13
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 22:52:57

Label at a glance#

ProductP.O.V. Antibacterial Foaming Hand

Active ingredientBENZALKONIUM CHLORIDE

Label structure7 sections

Indications and uses

helps eliminate bacteria on hands.

Dosage and administration

Pump onto wet hands, rub into a rich foamy lather and rinse clean.

Storage and handling

store at room temperature.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

helps eliminate bacteria on hands.

Warnings

WARNINGS SECTION

For external use only.

When using this product

OTC - WHEN USING SECTION

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

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation or redness develops and lasts.

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 onto wet hands, rub into a rich foamy lather and rinse clean.

Other information

STORAGE AND HANDLING SECTION

store at room temperature.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Cocamidopropyl Betaine, Polysorbate 20, Fragrance (Parfum), Glyceirn, Decyl Glucoside, Hydroxyethylcellulose, Aloe Barbadensis Leaf Juice, Camellia Sinensis Leaf Extract, Polyquaternium-7, Tetrasodium EDTA, Sodium Citrate, Citric Acid, Benzophenone-4, Methylchloroisothiazolinone, Methylisothiazolinone, Yellow 5 (CI 19140), Red 33 (CI 17200).

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
1046593	benzalkonium chloride 0.13 % Medicated Liquid Soap	PSN	1
1046593	benzalkonium chloride 1.3 MG/ML Medicated Liquid Soap	SCD	1
1046593	benzalkonium chloride 0.13 % Medicated Liquid Soap	SY	1
1046593	benzalkonium chloride 1.33 MG/ML Medicated Liquid Soap	SY	1

Product Linked Resources#

Resource, Code type, Value table
Resource	Code type	Value	Equivalent identifiers	Source image
Barcode	EAN-13	0067153948535	GTIN-13: 0067153948535 EAN-13: 0067153948535 GTIN-12: 067153948535 UPC-A: 067153948535 GTIN storage (14 digits): 00067153948535	22786L.jpg

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
63148-197-08	2024-01-30	C162847	48780-1	1030e365-59fa-111a-e063-dadaa90a10e2	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
63148-197-08	P.O.V. Antibacterial Foaming Hand	222 mL in 1 BOTTLE, PLASTIC	SOAP	222		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
63148-197	P.O.V. ANTIBACTERIAL FOAMING HAND (BENZALKONIUM CHLORIDE) SOAP [APOLLO HEALTH AND BEAUTY CARE INC.]	1	Legacy NDC, 1 package rows	20171113_3e594ee5-3900-476f-87aa-91b046dcab12.zip

Products#

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

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

P.O.V. Antibacterial Foaming Hand
Benzalkonium Chloride
BENZALKONIUM
WATER
COCAMIDOPROPYL BETAINE
POLYSORBATE 20
GLYCERIN
DECYL GLUCOSIDE
HYDROXYETHYL CELLULOSE (5000 CPS AT 1%)
ALOE VERA LEAF
GREEN TEA LEAF
POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW)
EDETATE SODIUM
SODIUM CITRATE
CITRIC ACID MONOHYDRATE
SULISOBENZONE
METHYLCHLOROISOTHIAZOLINONE
METHYLISOTHIAZOLINONE
FD&C YELLOW NO. 5
D&C RED NO. 33

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
63148-197	63148-197-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB
WATER	059QF0KO0R	IACT
COCAMIDOPROPYL BETAINE	5OCF3O11KX	IACT
POLYSORBATE 20	7T1F30V5YH	IACT
GLYCERIN	PDC6A3C0OX	IACT
DECYL GLUCOSIDE	Z17H97EA6Y	IACT
HYDROXYETHYL CELLULOSE (5000 CPS AT 1%)	X70SE62ZAR	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
GREEN TEA LEAF	W2ZU1RY8B0	IACT
POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW)	0L414VCS5Y	IACT
EDETATE SODIUM	MP1J8420LU	IACT
SODIUM CITRATE	1Q73Q2JULR	IACT
CITRIC ACID MONOHYDRATE	2968PHW8QP	IACT
SULISOBENZONE	1W6L629B4K	IACT
METHYLCHLOROISOTHIAZOLINONE	DEL7T5QRPN	IACT
METHYLISOTHIAZOLINONE	229D0E1QFA	IACT
FD&C YELLOW NO. 5	I753WB2F1M	IACT
D&C RED NO. 33	9DBA0SBB0L	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
21d5146c-28a7-46fe-8a31-c8e129d418ec			3e594ee5-3900-476f-87aa-91b046dcab12	2017-11-13	Warnings	Exact identifier spl id: 21d5146c-28a7-46fe-8a31-c8e129d418ec spl set id: 3e594ee5-3900-476f-87aa-91b046dcab12

Reported adverse events (FAERS/openFDA)#

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