INSTANT HAND SANITIZER

Manufacturer: FOSHAN KANGKANG BIOTECHNOLOGY?CO.,LTD
Effective date: 2020-06-09
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:16:53

Label at a glance#

ProductINSTANT HAND SANITIZER

Active ingredientALCOHOL

Label structure11 sections

Dosage and administration

Place enough product on hands to cover all surfaces. Rub hands together until dry. Children under 6 years of age should be supervised when using this product.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 71% v/v

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria that potentially can cause disease

Warnings

WARNINGS SECTION

For external use only; Do not eat ;Flammable,keep away from fire

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.

Children under 6 years of age should be supervised when using this product.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Glycerin

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

30 ml label500 ml label1 L label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
2282911	ethanol 71 % Topical Gel	PSN	1
2282911	ethanol 0.71 ML/ML Topical Gel	SCD	1
2282911	ethanol 71 % Topical Gel	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
78413-001-01	2022-01-28	C162847	48780-1	d6a99b39-c1f2-a426-e053-dadaa90af4c2	INSTANT HAND SANITIZER
78413-001-02	2022-01-28	C162847	48780-1	d6a99b39-c1f2-a426-e053-dadaa90af4c2	INSTANT HAND SANITIZER
78413-001-03	2022-01-28	C162847	48780-1	d6a99b39-c1f2-a426-e053-dadaa90af4c2	INSTANT HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
78413-001-01	INSTANT HAND SANITIZER	30 mL in 1 BOTTLE	GEL	30	1
78413-001-02	INSTANT HAND SANITIZER	500 mL in 1 BOTTLE	GEL	500	1
78413-001-03	INSTANT HAND SANITIZER	1000 mL in 1 BOTTLE	GEL	1000	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
78413-001	INSTANT HAND SANITIZER GEL [FOSHAN KANGKANG BIOTECHNOLOGY?CO.,LTD]	1	Legacy NDC, 3 package rows	20200610_a7a3c8f7-0010-1f6f-e053-2a95a90a81a7.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

INSTANT HAND SANITIZER
GLYCERIN
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
78413-001	78413-001-01, 78413-001-02, 78413-001-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
GLYCERIN	PDC6A3C0OX	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
a7a3e591-dd0c-7b2b-e053-2995a90a5fe2			a7a3c8f7-0010-1f6f-e053-2a95a90a81a7	2020-06-09	Warnings	Exact identifier spl id: a7a3e591-dd0c-7b2b-e053-2995a90a5fe2 spl set id: a7a3c8f7-0010-1f6f-e053-2a95a90a81a7

Reported adverse events (FAERS/openFDA)#

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