LOCKE TEDDY- alcohol antiseptic gel

LOCKE TEDDY by

Drug Labeling and Warnings

LOCKE TEDDY 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]

Active lngredient  

 Alcohol 75% v/v

Purpose 

Anti-Bacterial

Uses 

Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings  

For external use only. Flammable. Keep away from heat or flame
Do not use
in children less than 2 months of age
on open skin wounds
When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing

Other information

Store between 15-30°C (59-86F)

Avoid freezing and excessively heat above 40°C (104F)

Inactives 

Glycerin, Carbome, hydrogen peroxide, Purified Water USP

KEEP OUT OF REACH OF CHILDREN

Product Label

INGREDIENTS AND APPEARANCE

LOCKE TEDDY 
alcohol antiseptic gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73928-001
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
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
WATER (UNII: 059QF0KO0R)
CARBOMER 980 (UNII: 4Q93RCW27E)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73928-001-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/26/2020
2	NDC: 73928-001-02	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/26/2020
3	NDC: 73928-001-03	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/26/2020
4	NDC: 73928-001-04	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/26/2020
5	NDC: 73928-001-05	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/26/2020
6	NDC: 73928-001-06	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/26/2020
7	NDC: 73928-001-07	2000 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/26/2020
8	NDC: 73928-001-08	200 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/26/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/26/2020

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(73928-001)