ER-KANG INSTANT HAND SANITIZER- alcohol liquid

Er-Kang Instant Hand Sanitizer by

Drug Labeling and Warnings

Er-Kang Instant Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Hunan Er-Kang Pharmaceutical Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Ethyl Alcohol 75% (v/v)

Purpose

Antimicrobial

USE:

Suitable for hand, skin sanitization

Warnings:

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

• 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

• irritation or redness occurs.

Keep out of reach of children's reach.

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

Directions

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:

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

Expiry Date:

Inactive Ingredients:

Purified Water

​Package Labeling: 100 mL 76165-0002-1

Package Labeling: 500 mL 76165-0002-2

Package Labeling: 1000 mL 76165-0002-3

INGREDIENTS AND APPEARANCE

ER-KANG INSTANT HAND SANITIZER 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76165-0002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.75 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76165-0002-1	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/24/2020
2	NDC: 76165-0002-2	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/24/2020
3	NDC: 76165-0002-3	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/24/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	02/24/2020

Labeler - Hunan Er-Kang Pharmaceutical Co., Ltd (529353518)