Royal Non-Alcohol Foam Hand Sanitizer

Manufacturer: CWGC LA Inc.
Effective date: 2023-09-21
Label type: HUMAN OTC DRUG LABEL
Version: 12
Source: full-release
Hydrated at: 2026-06-01 00:04:10

Label at a glance#

ProductRoyal Non-Alcohol Foam Hand Sanitizer

Active ingredientBENZALKONIUM CHLORIDE

Label structure7 sections

Indications and uses

For handwashing to reduce bacteria on the skin. Recommended for repeated use.

Dosage and administration

Apply foam sanitizer to hands. Rub over surfaces of both hands for 15 seconds. No rinsing required.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

BENZALKONIUM CHLORIDE 0.13%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

For handwashing to reduce bacteria on the skin. Recommended for repeated use.

Warnings

WARNINGS SECTION

For external use only

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

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develops and persists.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply foam sanitizer to hands.
Rub over surfaces of both hands for 15 seconds.
No rinsing required.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Coco-Glucoside, Laurtrimonium Chloride, Cocamidopropylamine Oxide, Citric Acid, Fragrance.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Royal Product_Labels_Non-Alc Foam Hand Sanitizer

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1020365	benzalkonium chloride 0.13 % Topical Foam	PSN	12
1020365	benzalkonium chloride 1.3 MG/ML Topical Foam	SCD	12
1020365	benzalkonium chloride 0.13 % Topical Foam	SY	12

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
3c386306-c48a-413e-bb69-70cb268496f3	Product name	1	20210727

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
70415-205-01	2025-01-30	C162847	48780-1	0191ceaa-64d5-198a-e063-dbdaa90aec3e	CWGC (as PLD) - Royal Non-Alcohol Foam Hand Sanitizer (70415-205)
70415-205-01	2023-12-13	C162847	48780-1	0191ceaa-64d5-198a-e063-dbdaa90aec3e	CWGC (as PLD) - Royal Non-Alcohol Foam Hand Sanitizer (70415-205)
70415-205-01	2023-07-28	C162847	48780-1	0191ceaa-64d5-198a-e063-dbdaa90aec3e	CWGC (as PLD) - Royal Non-Alcohol Foam Hand Sanitizer (70415-205)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
70415-205-01	Royal Non-Alcohol Foam Hand Sanitizer	1000 mL in 1 BOTTLE	SOLUTION	1000		12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
70415-205	ROYAL NON-ALCOHOL FOAM HAND SANITIZER (BENZALKONIUM CHLORIDE) SOLUTION [CWGC LA INC.]	12	Legacy NDC, 1 package rows	20231214_05364f49-c8a9-41a3-a536-9cc2f53bb884.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

Royal Non-Alcohol Foam Hand Sanitizer
Benzalkonium Chloride
WATER
PROPYLENE GLYCOL
COCAMIDOPROPYL BETAINE
COCAMINE OXIDE
EDETATE DISODIUM
DMDM HYDANTOIN
TROLAMINE
FD&C YELLOW NO. 5
FD&C BLUE NO. 1
BENZALKONIUM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
70415-205	70415-205-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
COCAMIDOPROPYL BETAINE	5OCF3O11KX	IACT
COCAMINE OXIDE	QWA2IZI6FI	IACT
EDETATE DISODIUM	7FLD91C86K	IACT
DMDM HYDANTOIN	BYR0546TOW	IACT
TROLAMINE	9O3K93S3TK	IACT
FD&C YELLOW NO. 5	I753WB2F1M	IACT
FD&C BLUE NO. 1	H3R47K3TBD	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
05df979c-9693-55f4-e063-6294a90a1613			05364f49-c8a9-41a3-a536-9cc2f53bb884	2023-09-21	Warnings	Exact identifier spl id: 05df979c-9693-55f4-e063-6294a90a1613 spl set id: 05364f49-c8a9-41a3-a536-9cc2f53bb884

Reported adverse events (FAERS/openFDA)#

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