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Shunfa Anti-Bacteria Spra

Dosage form: spray
Ingredients: DIDECYLDIMETHYLAMMONIUM 3mg in 1000mg, TRICLOSAN 3mg in 1000mg, BENZALKONIUM BROMIDE 3mg in 1000mg, BORNEOL 4mg in 1000mg
Labeler: Chengdu Shunfa Disinfection and Washing Technology Co Ltd
NDC Code: 58686-013

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

SHUNFA ANTI-BACTERIA SPRAY

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

SHUNFA ANTI-BACTERIA SPRA 
didecyldimethyl ammonium,triclosan, borneol, benzalkonium bromide spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58686-013
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIDECYLDIMETHYLAMMONIUM (DIDECYLDIMETHYLAMMONIUM) DIDECYLDIMETHYLAMMONIUM3 mg  in 1000 mg
TRICLOSAN (TRICLOSAN) TRICLOSAN3 mg  in 1000 mg
BENZALKONIUM BROMIDE (BENZALKONIUM BROMIDE) BENZALKONIUM BROMIDE3 mg  in 1000 mg
BORNEOL (BORNEOL) BORNEOL4 mg  in 1000 mg
Inactive Ingredients
Ingredient NameStrength
POLYETHYLENE GLYCOL 1000100 mg  in 1000 mg
MENTHOL3 mg  in 1000 mg
WATER800 mg  in 1000 mg
Packaging
#Item CodePackage Description
1NDC:58686-013-0130 mg in 1 BOTTLE, SPRAY
2NDC:58686-013-025 mg in 1 BOTTLE, SPRAY
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A10/30/2005
Labeler - Chengdu Shunfa Disinfection and Washing Technology Co Ltd (527046468)
Registrant - Chengdu Shunfa Disinfection and Washing Technology Co Ltd (527046468)
Establishment
NameAddressID/FEIOperations
Chengdu Shunfa Disinfection and Washing Technology Co Ltd527046468manufacture(58686-013)

 
Chengdu Shunfa Disinfection and Washing Technology Co Ltd

Medically reviewed on Jun 5, 2018

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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