FDA.reportPublic FDA data

Er-Kang Instant Hand Sanitizer

Manufacturer
Hunan Er-Kang Pharmaceutical Co., Ltd
Effective date
2020-04-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:35:43

Label at a glance#

ProductEr-Kang Instant Hand Sanitizer
Active ingredientALCOHOL
Label structure9 sections

Dosage and administration

Wet hands thoroughly with product and rub into sin until dry.  Children under 6 years of age should be supervised by an adult when using.

Storage and handling

Store below 43 o C (110 o F)                           ​Batch No: Keep saled after use                                    ​Production Date: Expiry Date:

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75% (v/v)

Purpose

OTC - PURPOSE SECTION

Antimicrobial

USE:

INDICATIONS & USAGE SECTION

Suitable for hand, skin sanitization

Warnings:

WARNINGS SECTION

  1. External use, not oral.  Keep out of children's reach.
  2. Flammable, Keep away from fire and flame.
  3. Use with caution if allergic to alcohol.

When using this product

OTC - WHEN USING SECTION

  • Avoid contacting face, eyes and broken skin.  In case of eye contact, flush with plenty of water and seek medical advice.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • irritation or redness occurs.

Keep out of reach of children's reach.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a poison control center.

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and rub into sin until dry.  Children under 6 years of age should be supervised by an adult when using.

Other Information:

STORAGE AND HANDLING SECTION

  • Store below 43 oC (110 oF)                           ​Batch No:
  • Keep saled after use                                    ​Production Date:

Expiry Date:

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Purified Water

​Package Labeling: 100 mL 76165-0002-1

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

100100

Package Labeling: 500 mL 76165-0002-2

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

500500

Package Labeling: 1000 mL 76165-0002-3

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1000mL1000mL

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76165-000276165-0002-1, 76165-0002-2, 76165-0002-3

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
NameUNIIKind
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
c3f63a66-42ea-179c-e053-2a95a90ac1faa37246a2-eb01-44a9-bf35-912348b4aae62021-06-04WarningsExact identifier
spl set id: a37246a2-eb01-44a9-bf35-912348b4aae6

Reported adverse events (FAERS/openFDA)#

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