Pacific Breeze Instant Hand Sanitizer Gel

Manufacturer: Whisk Products, Inc.
Effective date: 2023-12-08
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-06-01 00:03:41

Label at a glance#

ProductPacific Breeze Instant Hand Sanitizer Gel

Active ingredientALCOHOL

Label structure7 sections

Dosage and administration

Place 5 grams or palmful of product in one hand. Spread on hands and run into skin until dry. Place a smaller amount (2.5) grams in one hand and spread over both hands and wrists. Rub into skin until dry. Children should be supervised while using this product.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 60% v/v

Purpose

OTC - PURPOSE SECTION

Skin Sanitizer

Use

INDICATIONS & USAGE SECTION

To help reduce the amount of bacteria on skin

Warnings

WARNINGS SECTION

Flammable. Keep away from fire or flame.

For external use only. If swallowed, seek medical attention.

When using this product do not use around or near the eyes. If contact occurs, flush eyes with water and contact a doctor immediately.

Stop use and consult a doctor when skin irritation appears and lasts.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

Directions

DOSAGE & ADMINISTRATION SECTION

Place 5 grams or palmful of product in one hand.
Spread on hands and run into skin until dry.
Place a smaller amount (2.5) grams in one hand and spread over both hands and wrists.
Rub into skin until dry.
Children should be supervised while using this product.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Fragrance, Carbomer, Propylene Glycol, Diisopropylamine

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label for 6 x 1000 mL Bags

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581658	ethanol 60 % Topical Gel	PSN	2
581658	ethanol 0.6 ML/ML Topical Gel	SCD	2
581658	ethanol 60 % Topical Gel	SY	2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
65585-380-01	Pacific Breeze Instant Hand Sanitizer Gel	6 in 1 BOX	GEL	6		2
65585-380-01	Pacific Breeze Instant Hand Sanitizer Gel	1 L in 1 BAG	GEL	1		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
65585-380	PACIFIC BREEZE INSTANT HAND SANITIZER GEL (ALCOHOL) GEL [WHISK PRODUCTS, INC.]	2	Current NDC, 2 package rows	20231209_3f574300-b05a-4f98-98fa-dd2177bb3d75.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

Pacific Breeze Instant Hand Sanitizer Gel
Alcohol
WATER
GLYCERIN
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)
PROPYLENE GLYCOL
DIISOPROPYLAMINE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
65585-380	65585-380-01

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
GLYCERIN	PDC6A3C0OX	IACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)	59TL3WG5CO	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
DIISOPROPYLAMINE	BR9JLI40NO	IACT
ALCOHOL	3K9958V90M	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
Pacific Breeze Instant Hand Sanitizer Gel	ALCOHOL	Whisk Products, Inc.	3f574300-b05a-4f98-98fa-dd2177bb3d75	2023-12-08	Warnings	Exact identifier ndc (package): 65585-380-01 ndc (product): 65585-380 ndc11 (package): 65585038001 spl id: 0c054670-1e49-d10b-e063-6294a90a7014 spl set id: 3f574300-b05a-4f98-98fa-dd2177bb3d75

Reported adverse events (FAERS/openFDA)#

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