ALCOHOL FREE HAND SANITIZER liquid

Alcohol Free Hand Sanitizer by

Drug Labeling and Warnings

Alcohol Free Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Fujian Jinghua Biotechnology Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Polyaminopropyl Biguanide 0.28%,Benzalkonium Chloride 0.13%

Purpose

Antiseptic

USES

For personal hand sanitizing and reduce bacteria on the skin,Recommended for repeated use.

Warnings

For external use only

When Using This Product

When Using This Product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water. Stop use and ask a doctor if irritation and redness develop. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

Directions

Apply liberally to the hands and gently rub to dry.

Inactive ingredients

Aqua(Water), Glycerin, Hydroxypropyl Methylcellulose, Sodium Benzoate, PEG/Ppg-17/6 Copolymer, Parfum, Disodium EDTA

Do not use

STOP USE

KEEP OUT OF REACH OF CHILDREN

STORAGE AND HANDLING

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

ALCOHOL FREE HAND SANITIZER 
alcohol free hand sanitizer liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75438-005
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100 mL
POLYAMINOPROPYL BIGUANIDE (UNII: DT9D8Z79ET) (POLYAMINOPROPYL BIGUANIDE - UNII:DT9D8Z79ET)	POLYAMINOPROPYL BIGUANIDE	0.28 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	5 g  in 100 mL
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)	1.5 g  in 100 mL
WATER (UNII: 059QF0KO0R)
BENZYL ALCOHOL (UNII: LKG8494WBH)	0.3 g  in 100 mL
PPG-17 (UNII: OV0Q322E0U)	0.5 g  in 100 mL
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)	0.08 g  in 100 mL
SODIUM BENZOATE (UNII: OJ245FE5EU)	0.6 g  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75438-005-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/25/2020
2	NDC: 75438-005-02	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/25/2020
3	NDC: 75438-005-03	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/25/2020
4	NDC: 75438-005-04	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/25/2020
5	NDC: 75438-005-05	300 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/25/2020
6	NDC: 75438-005-06	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/25/2020
7	NDC: 75438-005-07	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/25/2020
8	NDC: 75438-005-08	5000 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/25/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/25/2020

Labeler - Fujian Jinghua Blotechnology Co.,Ltd. (416242797)

Establishment
Name	Address	ID/FEI	Business Operations
Fujian Jinghua Blotechnology Co.,Ltd.		416242797	manufacture(75438-005)