Sanitizer

Manufacturer: Gandang Kalikasan USA Inc.
Effective date: 2018-12-31
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-05-31 22:58:03

Label at a glance#

ProductSanitizer

Active ingredientALCOHOL

Label structure8 sections

Indications and uses

Uses: Helps decrease bacteria on skin Recommended for repeated use

Dosage and administration

Directions: Shake well.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

Ethyl alcohol 60%

Uses:

INDICATIONS & USAGE SECTION

Uses:

Helps decrease bacteria on skin
Recommended for repeated use

Purpose

OTC - PURPOSE SECTION

Purpose

Antiseptic

Warnings

WARNINGS SECTION

Warnings

For external use only. Avoid contact with eyes. If contact occurs, rinse with water.

Flammable, keep away from fire or flame.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contat a Poison Control Center right away.

For children under 6, use only under adult supervision. Not recommended for infants.

Directions

INSTRUCTIONS FOR USE SECTION

Directions:

Shake well.

DOSAGE & ADMINISTRATION SECTION

Spray onto hands and rub thorughly.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Inactive ingredients

aqua (water), Mentha piperita (peppermint) leaf essential oil, Mentha arvensis (corn mint) leaf essential oil, Aloe barbadensis leaf juice

Principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Cool Burst drug facts

All-Natural Sanitizer Cool Burst 50ml PDP

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1367692	ethanol 60 % Topical Spray	PSN	3
1367692	ethanol 0.6 ML/ML Topical Spray	SCD	3
1367692	ethanol 60 % Topical Spray	SY	3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
70143-1002-1	2021-01-29	C162847	48780-1	ba0f9c33-0f37-a910-e053-dadaa90a0b85	All-Natural Sanitizer Cool Burst

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
70143-1002-1	Sanitizer	50 mL in 1 BOTTLE, SPRAY	SPRAY	50		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
70143-1002	SANITIZER (ALCOHOL) SPRAY [GANDANG KALIKASAN USA INC.]	3	Legacy NDC, 1 package rows	20190102_2673004f-68eb-01df-e054-00144ff8d46c.zip

Products#

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

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

Sanitizer
Alcohol
WATER
ALOE VERA LEAF
PEPPERMINT OIL
MENTHA ARVENSIS LEAF

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
70143-1002	70143-1002-1

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
WATER	059QF0KO0R	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
ALCOHOL	3K9958V90M	ACTIB
PEPPERMINT OIL	AV092KU4JH	IACT
MENTHA ARVENSIS LEAF	A4IWO4DDZ9	IACT

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
7e540eb8-e899-7be4-e053-2a91aa0ac08f			2673004f-68eb-01df-e054-00144ff8d46c	2018-12-31	Warnings	Exact identifier spl id: 7e540eb8-e899-7be4-e053-2a91aa0ac08f spl set id: 2673004f-68eb-01df-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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