WASHING-FREE HAND SANITIZER- alcohol gel

Washing-free Hand Sanitizer by

Drug Labeling and Warnings

Washing-free Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Jiangxi Zhangshu Zhengkang Medicine Biotechnology Co.,ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Alcohol 70% v/v. Purpose: Antiseptic

Purpose

Antiseptic, Hand Sanitizer

Use

Hand Sanitizer to help reduce bacteria on the skin

Warnings

This product is a disinfectant for external use only. Flammable. Keep away from open flame and source of heat

Do not use

It is forbidden to take orally

WHEN USING

Avoid contact with the eyes. If contact occurs, flush eyes with water.

STOP USE

Discontinue use and consult a health-care practitioner if irritation develops.

KEEP OUT OF REACH OF CHILDREN

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

Directions

1. Hand sanitizing: Place some product in your palm to thoroughly cover your hands. Rub hands together briskly until dry. Chirldren under 6 years of age should be supervised when using this product. Use a part of your daily cleansing routine.

2. Surgical hand antisepsis: After surgical hand washing, place some product in your hands, forearm and upper arm 1/3 skin, rub them together briskly for 3-5 minutes, then can wear sterile golves.

Other information

• Store below 110F (43C).
• May discolor certain fabrics or surfaces

Inactive ingredients

Water (purified), Glycerin, Grape fruit extract, Honeysuckle extract, wormwood leaf extract, Aloe extract, Carbomer, Sodium hyaluronate, Triethanolamine, Propylene glycol

Package Label - Principal Display Panel

50 mL NDC: 74621-001-01

500 mL NDC: 74621-001-02

INGREDIENTS AND APPEARANCE

WASHING-FREE HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74916-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE (UNII: V5VD430YW9)
WORMWOOD (UNII: F84709P2XV)
TROLAMINE (UNII: 9O3K93S3TK)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
GLYCERIN (UNII: PDC6A3C0OX)	1.45 mL  in 100 mL
GRAPEFRUIT (UNII: O82C39RR8C)
WATER (UNII: 059QF0KO0R)
LONICERA JAPONICA FLOWER (UNII: 4465L2WS4Y)
PEG-9 DIGLYCIDYL ETHER/SODIUM HYALURONATE CROSSPOLYMER (UNII: 788QAG3W8A)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74916-001-01	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/08/2020
2	NDC: 74916-001-02	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/08/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/08/2020

Labeler - Jiangxi Zhangshu Zhengkang Medicine Biotechnology Co.,ltd. (541567296)

Establishment
Name	Address	ID/FEI	Business Operations
Jiangxi Zhangshu Zhengkang Medicine Biotechnology Co.,ltd.		541567296	manufacture(74916-001)