SHUNFA ANTI-BACTERIA SPRA- didecyldimethyl ammonium,triclosan, borneol, benzalkonium bromide spray

Shunfa Anti-Bacteria Spra by

Drug Labeling and Warnings

Shunfa Anti-Bacteria Spra by is a Otc medication manufactured, distributed, or labeled by Chengdu Shunfa Disinfection and Washing Technology Co Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS

Didecyldimethyl Ammonium 0.3%

Triclosan                              0.3%

Borneol                               0.4%

Benzalkonium Bromide       0.3%

PURPOSES

Antibacterial

KEEP OUT OF REACH OF CHILDREN.

If swallowed, get medical help or contact a Poison Control Center.

DO NOT USE

if you are allergic to any of the ingredients.

WHEN USING THIS DEVICE

do not get into eyes. If eye contact occurs, rinse thoroughly with water.

STOP USE AND ASK A DOCTOR IF

irritation or redness develops, and continues for more than 72 hours.

USES

Uses spray to reduce bacteria on the skin.

WARNINGS

For external use only.

DIRECTIONS

for adults and children 2 years and olde, apply to human body, allow to dry without wiping, ask a doctor before using on children under 2 years.

INACTIVE INGREDIENTS

Polyethylene Glycol, Menthol, Water

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SHUNFA ANTI-BACTERIA SPRA 
didecyldimethyl ammonium,triclosan, borneol, benzalkonium bromide spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58686-013
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DIDECYLDIMETHYLAMMONIUM (UNII: Z7F472XQPA) (DIDECYLDIMETHYLAMMONIUM - UNII:Z7F472XQPA)	DIDECYLDIMETHYLAMMONIUM	3 mg  in 1000 mg
TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X)	TRICLOSAN	3 mg  in 1000 mg
BENZALKONIUM BROMIDE (UNII: 151T1GQ42D) (BENZALKONIUM BROMIDE - UNII:151T1GQ42D)	BENZALKONIUM BROMIDE	3 mg  in 1000 mg
BORNEOL (UNII: M89NIB437X) (BORNEOL - UNII:M89NIB437X)	BORNEOL	4 mg  in 1000 mg

Inactive Ingredients
Ingredient Name	Strength
POLYETHYLENE GLYCOL 1000 (UNII: U076Q6Q621)	100 mg  in 1000 mg
MENTHOL (UNII: L7T10EIP3A)	3 mg  in 1000 mg
WATER (UNII: 059QF0KO0R)	800 mg  in 1000 mg

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 58686-013-01	30 mg in 1 BOTTLE, SPRAY
2	NDC: 58686-013-02	5 mg in 1 BOTTLE, SPRAY

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	10/30/2005

Labeler - Chengdu Shunfa Disinfection and Washing Technology Co Ltd (527046468)

Registrant - Chengdu Shunfa Disinfection and Washing Technology Co Ltd (527046468)

Establishment
Name	Address	ID/FEI	Business Operations
Chengdu Shunfa Disinfection and Washing Technology Co Ltd		527046468	manufacture(58686-013)