Sani-Kure Extra Strength Hand Sanitizer

Manufacturer: KOLORCURE CORPORATION
Effective date: 2022-01-19
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:47:13

Label at a glance#

ProductSani-Kure Extra Strength Hand Sanitizer

Active ingredientALCOHOL

Label structure10 sections

Dosage and administration

Place enough product in your palm to cover hands. Rub hands together until dry. Children under 6 years of age should be supervised when using Sani-Kure.

Storage and handling

Do not store above 110°F.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% v/v. Purpose: Antimicrobial

Use:

OTC - PURPOSE SECTION

Antimicrobial

Warnings

WARNINGS SECTION

Flammable. Keep away from heat or flame. Harmful if swallowed. For external use only.

Do not use

OTC - DO NOT USE SECTION

in or around the eys.

OTC - WHEN USING SECTION

In case of contact immediately flush eyes with water.

If swallowed, contact physician.

Keep out of reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

Place enough product in your palm to cover hands. Rub hands together until dry.
Children under 6 years of age should be supervised when using Sani-Kure.

Other information

STORAGE AND HANDLING SECTION

Do not store above 110°F.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Pure Aloe Vera, vegetable glycerin, isopropyl alcohol, hydrogen peroxide, distilled water.

Warnings

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

2 FL OZ (59 mL)

2 oz Front Panel2 oz Drug Panel

2 oz Side Panel

4 FL OZ (118 mL)

4 oz Front

4 oz Drug Panel

8 oz (236 mL)

8 oz Front

8 oz Drug Panel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
78923-001-04	2023-07-28	C162847	48780-1	0191ceaa-6884-198a-e063-dbdaa90aec3e	a932b278-ee8a-c37a-e053-2995a90aa2a1
78923-001-08	2023-07-28	C162847	48780-1	0191ceaa-6884-198a-e063-dbdaa90aec3e	a932b278-ee8a-c37a-e053-2995a90aa2a1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
78923-001-04	Sani-Kure Extra Strength Hand Sanitizer	118 mL in 1 BOTTLE, SPRAY	SOLUTION	118		2
78923-001-08	Sani-Kure Extra Strength Hand Sanitizer	236 mL in 1 BOTTLE, SPRAY	SOLUTION	236		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
78923-001	SANI-KURE EXTRA STRENGTH HAND SANITIZER (ALCOHOL) SOLUTION [KOLORCURE CORPORATION]	2	Legacy NDC, 2 package rows	20220120_a932b278-ee8a-c37a-e053-2995a90aa2a1.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

Sani-Kure Extra Strength Hand Sanitizer
ALCOHOL
ALOE VERA WHOLE
GLYCERIN
HYDROGEN PEROXIDE
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
78923-001	78923-001-04, 78923-001-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALOE VERA WHOLE	KIZ4X2EHYX	IACT
GLYCERIN	PDC6A3C0OX	IACT
HYDROGEN PEROXIDE	BBX060AN9V	IACT
WATER	059QF0KO0R	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
d5f4878d-f212-a454-e053-2995a90a700b			a932b278-ee8a-c37a-e053-2995a90aa2a1	2022-01-19	Warnings	Exact identifier spl id: d5f4878d-f212-a454-e053-2995a90a700b spl set id: a932b278-ee8a-c37a-e053-2995a90aa2a1

Reported adverse events (FAERS/openFDA)#

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