Sunna Pure Hand Sanitizer Gel

Manufacturer: Spa Dent Inc.
Effective date: 2021-01-04
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:36:24

Label at a glance#

ProductSunna Pure Hand Sanitizer Gel

Active ingredientALCOHOL

Label structure7 sections

Dosage and administration

• Place enough product on hands to cover all surfaces. Rub hands together until dry. • Supervise children under 6 years of age when using this product to avoid swallowing.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% v/v

PURPOSE

OTC - PURPOSE SECTION

Antiseptic

USE(S)

INDICATIONS & USAGE SECTION

• Antiseptic (skin) cleanser • Medicated (skin) cleanser • Antibacterial (skin) cleanser • Effective in destroying (harmful) bacteria to provide antiseptic cleansing • For personal hand hygiene to help prevent the spread of bacteria

WARNINGS

WARNINGS SECTION

• For external use only. Flammable. Keep away from heat or flame.

Do not use

OTC - DO NOT USE SECTION

• in children less than 2 months of age • on open skin wounds.

When using this product

OTC - WHEN USING SECTION

• keep out of eyes, ears, and mouth • In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation or rash occurs. These may be signs of a serious condition.

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

• Place enough product on hands to cover all surfaces. Rub hands together until dry. • Supervise children under 6 years of age when using this product to avoid swallowing.

OTHER INFORMATION

SPL UNCLASSIFIED SECTION

• Store between 15° - 30° C (59° - 86° F) out of direct sunlight • Avoid freezing and excessive heat above 40° C (104° F).

Do not use this product if tamper-resistant seal is broken when opened.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Purified Water, Aloe Barbadensis Leaf Juice, Vitamin E, Glycerin, Carbomer Copolymer, Aminomethyl Propanol

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581662	ethanol 70 % Topical Gel	PSN	2
581662	ethanol 0.7 ML/ML Topical Gel	SCD	2
581662	ethanol 70 % Topical Gel	SY	2
581662	ethyl alcohol 70 % Topical Gel	SY	2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
79147-003-01	2024-01-30	C162847	48780-1	1030e365-68b8-111a-e063-dadaa90a10e2	Sunna Pure Hand Sanitizer Gel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
79147-003-01	Sunna Pure Hand Sanitizer Gel	946 mL in 1 BOTTLE, PUMP	GEL	946		2
79147-003-01	Sunna Pure Hand Sanitizer Gel	6 in 1 CASE	GEL	6		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
79147-003	SUNNA PURE HAND SANITIZER GEL (ALCOHOL) GEL [SPA DENT INC.]	2	Legacy NDC, 2 package rows	20210105_76e0d524-1333-464e-a2e5-6c06356ca6ba.zip

Products#

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

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

Sunna Pure Hand Sanitizer Gel
ALCOHOL
WATER
ALOE VERA LEAF
.ALPHA.-TOCOPHEROL
GLYCERIN
AMINOMETHYLPROPANOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
79147-003	79147-003-01

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
ALOE VERA LEAF	ZY81Z83H0X	IACT
.ALPHA.-TOCOPHEROL	H4N855PNZ1	IACT
GLYCERIN	PDC6A3C0OX	IACT
AMINOMETHYLPROPANOL	LU49E6626Q	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
b815414a-c34b-ec23-e053-2995a90abfae			76e0d524-1333-464e-a2e5-6c06356ca6ba	2021-01-04	Warnings	Exact identifier spl id: b815414a-c34b-ec23-e053-2995a90abfae spl set id: 76e0d524-1333-464e-a2e5-6c06356ca6ba

Reported adverse events (FAERS/openFDA)#

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