Antibacterial Hand Sanitizer

Manufacturer: CVS Pharmacy Inc | Apollo Health and Beauty Care
Effective date: 2010-10-08
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 22:26:04

Label at a glance#

ProductAntibacterial Hand Sanitizer Sunblossom

Active ingredientALCOHOL

Label structure8 sections

Indications and uses

To help reduce bacteria on the skin

Dosage and administration

Wet hands thoroughly and rub together until dry

Storage and handling

Store at a temperature below 110 o F (43 o C)

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol %62

Purpose

OTC - PURPOSE SECTION

Antiseptic

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly and rub together until dry

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. If contact occurs, rinse with water

Stop using this product and ask 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

Uses

INDICATIONS & USAGE SECTION

To help reduce bacteria on the skin

Other information

STORAGE AND HANDLING SECTION

Store at a temperature below 110^oF (43^oC)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Propylene Glycol, Carbomer, Glycerin, Fragrance (Parfum), Isopropyl Myristate, Tocopheryl Acetate, Aminomethyl Propanol, Mannitol, Cellulose, Hydroxypropyl Methylcellulose, Mica, Titanium Dioxide (CI 77891), Iron Oxides (CI 77492), Iron Oxides (CI 77491), Yellow 5 (CI 19140), Yellow 6 (CI 15985).

Package Front and Back Labels

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

2OZ Front and Back Labels: eb2.jpg2OZ Front and Back Labels

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581660	ethanol 62 % Topical Gel	PSN	1
581660	ethanol 0.62 ML/ML Topical Gel	SCD	1
581660	ethanol 62 % Topical Gel	SY	1

Product Linked Resources#

Resource, Code type, Value table
Resource	Code type	Value	Equivalent identifiers	Source image
Barcode	EAN-13	0050428732670	GTIN-13: 0050428732670 EAN-13: 0050428732670 GTIN-12: 050428732670 UPC-A: 050428732670 GTIN storage (14 digits): 00050428732670	eb2.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
59779-261-02	2020-01-31	C162847	48780-1	9d75b9d0-b4e2-f424-e053-dadaa90a57ce	Drug Facts Box - Back Label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
59779-261-02	Antibacterial Hand SanitizerSunblossom	59 mL in 1 BOTTLE, PLASTIC	GEL	59		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
59779-261	ANTIBACTERIAL HAND SANITIZER SUNBLOSSOM (ALCOHOL) GEL [CVS PHARMACY INC]	1	Legacy NDC, 1 package rows	20101008_f25ca2aa-7a7d-41f8-a9e4-ac1f70afb357.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version	Uploaded
ALCOHOL	ACTIVE INGREDIENT	3K9958V90M	1
ALCOHOL	ACTIVE MOIETY	3K9958V90M	1

Products#

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

DailyMed product names page 1 of 1 · 2 matching rows.

Antibacterial Hand Sanitizer Sunblossom
Alcohol

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
59779-261	59779-261-02

Ingredients#

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

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

Name, UNII, Kind table
Name	UNII	Kind
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
b01940dc-a0a4-4ff2-8803-58bebb68cf3e			f25ca2aa-7a7d-41f8-a9e4-ac1f70afb357	2010-10-08	Warnings	Exact identifier spl id: b01940dc-a0a4-4ff2-8803-58bebb68cf3e spl set id: f25ca2aa-7a7d-41f8-a9e4-ac1f70afb357

Reported adverse events (FAERS/openFDA)#

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