Royal 70-percent Alcohol Foam Hand Sanitizer

Manufacturer: CWGC LA Inc.
Effective date: 2023-09-21
Label type: HUMAN OTC DRUG LABEL
Version: 10
Source: full-release
Hydrated at: 2026-06-01 00:04:15

Label at a glance#

ProductRoyal 70-percent Alcohol Foam Hand Sanitizer

Active ingredientALCOHOL

Label structure7 sections

Indications and uses

For sanitizing to reduce bacteria on the skin.

Dosage and administration

Apply one shot of foaming sanitizer to dry hands Rub into skin No rinsing required

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70 %

Purpose

OTC - PURPOSE SECTION

Antibacterial

PURPOSE

OTC - PURPOSE SECTION

ANTIBACTERIAL

Uses

INDICATIONS & USAGE SECTION

For sanitizing to reduce bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only

Flammable :Keep away from fire or flame

When using this product

OTC - WHEN USING SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

Apply one shot of foaming sanitizer to dry hands
Rub into skin
No rinsing required

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Isopropyl Alcohol, Propylene Glycol, PEG-12 Dimethicone Crosspolymer, BIS-PEG-12 Dimethicone.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Royal Product_Labels_70pct Alcohol Foam Hand Sanitizer

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
616805	ethanol 70 % Topical Foam	PSN	10
616805	ethanol 0.7 ML/ML Topical Foam	SCD	10
616805	ethanol 70 % Topical Foam	SY	10

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
70415-202-01	2025-01-30	C162847	48780-1	0191ceaa-6671-198a-e063-dbdaa90aec3e	CWGC (as PLD) - Royal 70% Alcohol Foam Hand Sanitizer (70415-202)
70415-202-01	2023-12-13	C162847	48780-1	0191ceaa-6671-198a-e063-dbdaa90aec3e	CWGC (as PLD) - Royal 70% Alcohol Foam Hand Sanitizer (70415-202)
70415-202-01	2023-07-28	C162847	48780-1	0191ceaa-6671-198a-e063-dbdaa90aec3e	CWGC (as PLD) - Royal 70% Alcohol Foam Hand Sanitizer (70415-202)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
70415-202-01	Royal 70-percent Alcohol Foam Hand Sanitizer	1000 mL in 1 BOTTLE	LIQUID	1000		10

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
70415-202	ROYAL 70-PERCENT ALCOHOL FOAM HAND SANITIZER (ETHYL ALCOHOL) LIQUID [CWGC LA INC.]	10	Legacy NDC, 1 package rows	20231214_bc650f09-3539-4cb9-8f56-332090d2bc39.zip

Products#

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

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

Royal 70-percent Alcohol Foam Hand Sanitizer
ETHYL ALCOHOL
WATER
ISOPROPYL ALCOHOL
PROPYLENE GLYCOL
PEG-12 DIMETHICONE (300 CST)
BIS-PEG-12 DIMETHICONE (70 MPA.S)
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
70415-202	70415-202-01

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
WATER	059QF0KO0R	IACT
ISOPROPYL ALCOHOL	ND2M416302	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
PEG-12 DIMETHICONE (300 CST)	ZEL54N6W95	IACT
BIS-PEG-12 DIMETHICONE (70 MPA.S)	2JDK5W22H4	IACT
ALCOHOL	3K9958V90M	ACTIB

Source Document#

Source XML · Source PDF

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
05df95b5-e64c-13ab-e063-6394a90ab8ea			bc650f09-3539-4cb9-8f56-332090d2bc39	2023-09-21	Warnings	Exact identifier spl id: 05df95b5-e64c-13ab-e063-6394a90ab8ea spl set id: bc650f09-3539-4cb9-8f56-332090d2bc39

Reported adverse events (FAERS/openFDA)#

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