LOCKE TEDDY FOAMING HAND SANITIZER- benzalkonium chloride solution

LOCKE TEDDY Foaming Hand Sanitizer by

Drug Labeling and Warnings

LOCKE TEDDY Foaming Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by KINGKEY MBC LIFE TECHNOLOGY GROUP CO., LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug facts

Active ingredient

Benzalkonium Chloride 0.1%

Purpose

Antimicrobial 

Uses

1. for hand sanitizing to decrease the bacteria on the skin
2. recommended for repeated use

Warnings

For external use only. 

When using this productavoid contact with eyes. In case of eye contact, flush eyes with water.

Stop use and ask a doctor ifirritation or redness develops, or if condition persists for more than 72 hours.

Keep out of reach of children

 if swallowed, get medical help or contact a Poison Control Center right away.

Directions

1. pump a small amount of foam into palm of hand 
2. rub thoroughly over all surfaces of both hands 
3. rub hands together briskly until dry 

Inactive ingredients

Water, cetrimonium chloride, Laurtrimonium chloride, Dihydroxyethyl Cocamine oxide, citric acid, glycereth-17 cocoate

Product label

INGREDIENTS AND APPEARANCE

LOCKE TEDDY FOAMING HAND SANITIZER 
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73928-011
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.1 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC)
DIHYDROXYETHYL COCAMINE OXIDE (UNII: 8AR51R3BL5)
GLYCERETH-17 COCOATE (UNII: 3057VPT0KC)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73928-011-01	30 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/23/2021
2	NDC: 73928-011-02	50 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/23/2021
3	NDC: 73928-011-03	60 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/23/2021
4	NDC: 73928-011-04	200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/23/2021
5	NDC: 73928-011-05	250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/23/2021
6	NDC: 73928-011-06	300 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/23/2021
7	NDC: 73928-011-07	400 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/23/2021
8	NDC: 73928-011-08	500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/23/2021
9	NDC: 73928-011-09	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/23/2021
10	NDC: 73928-011-10	2000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/23/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	03/23/2021

Labeler - KINGKEY MBC LIFE TECHNOLOGY GROUP CO., LTD (545349263)

Establishment
Name	Address	ID/FEI	Business Operations
KINGKEY MBC LIFE TECHNOLOGY GROUP CO., LTD		545349263	manufacture(73928-011)