M MARVEL SANI CARE MULTI FUNCTION DISINFECTANT LIQUID NO RINSE- benzalkonium chloride spray

M MARVEL SANI CARE Multi Function Disinfectant Liquid No Rinse by

Drug Labeling and Warnings

M MARVEL SANI CARE Multi Function Disinfectant Liquid No Rinse by is a Otc medication manufactured, distributed, or labeled by GUANGZHOU TECHIN DEVELOPMENT CO., LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Benzalkonium Chloride  0.02%

Purpose

Antiseptic

Use

For Daily and Surgical hand disinfection to reduce bacteria on hands

Warnings

For external use only.
Keep away from fires and high temperatures.

Do Not Use: On open skin wounds.

WHEN USING

When using this product: Avoid eyes.
In case of contact with eyes, rinse eyes thoroughly with water.

STOP USE

Stop use If irritation or rash occurs. If condition persists, contact a health care practitioner.

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

• Put proper amount (around 3ml) onto palm and rub hands briskly until dry.
• No washing or rinsing required. Air dries quickly.

Other information

Keep in closed container in a cool dry place of ambient temperature.
Batch and MFG date printed on bottle.
Validity: 24 months from MFG date.
MADE IN CHINA

Inactive ingredients

Didecyl Dimethyl Ammonium Chloride, Ethyl Alcohol, Disodium EDTA, Water

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

M MARVEL SANI CARE MULTI FUNCTION DISINFECTANT LIQUID NO RINSE 
benzalkonium chloride spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80107-003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.02 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)
DISODIUM HEDTA (UNII: KME849MC7A)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80107-003-01	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/21/2020
2	NDC: 80107-003-02	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/21/2020
3	NDC: 80107-003-03	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/21/2020
4	NDC: 80107-003-04	750 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/21/2020
5	NDC: 80107-003-05	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/21/2020
6	NDC: 80107-003-06	3785 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/21/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	12/21/2020

Labeler - GUANGZHOU TECHIN DEVELOPMENT CO., LTD (527219392)

Establishment
Name	Address	ID/FEI	Business Operations
GUANGZHOU TECHIN DEVELOPMENT CO., LTD		527219392	manufacture(80107-003)