SIMONIZ SANICLEAN- benzalkonium chloride soap

SIMONIZ SaniClean by

Drug Labeling and Warnings

SIMONIZ SaniClean by is a Otc medication manufactured, distributed, or labeled by Hangzhou Huiji Biotechnology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antibacterial

Use

For hand sanitizing to reduce bacteria
on the skin.

WARNINGS

For external use only
When using this product avoid contact with eyes.
In case of eye contact, flush with water.
Stop use and ask a doctor if irritation or redness
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

●Pump into hands, wet as needed.
●Lather vigorously for at least 15 seconds.
●Wash skin, rinse thoroughly and dry.

Inactive ingredients

water, cetrimonium
chloride, glycerin, lauramidopropylamine oxide, cocamide
MEA, sodium chloride, PEG-120 methyl glucose dioleate,
citric acid, tetrasodium EDTA, methylchloroisothiazolinone,
methylisothiazolinone.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SIMONIZ SANICLEAN 
benzalkonium chloride soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73788-106
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 g

Inactive Ingredients
Ingredient Name	Strength
PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)
EDETATE SODIUM (UNII: MP1J8420LU)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV)
COCO MONOETHANOLAMIDE (UNII: C80684146D)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73788-106-01	20 in 1 CARTON	07/15/2020
1		500 g in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC: 73788-106-02	8 in 1 CARTON	07/15/2020
2		1500 g in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	07/15/2020

Labeler - Hangzhou Huiji Biotechnology Co., Ltd. (526893497)

Establishment
Name	Address	ID/FEI	Business Operations
Hangzhou Huiji Biotechnology Co., Ltd.		526893497	manufacture(73788-106)