SHUNFA ANTI-BACTERIA SPRAY

Manufacturer: Chengdu Shunfa Disinfection and Washing Technology Co Ltd
Effective date: 2013-06-05
Label type: HUMAN OTC DRUG LABEL
Version: 2930
Source: full-release
Hydrated at: 2026-05-31 22:35:38

Label at a glance#

ProductShunfa Anti-Bacteria Spra

Active ingredientDIDECYLDIMETHYLAMMONIUM, TRICLOSAN, BENZALKONIUM BROMIDE, BORNEOL

Label structure11 sections

Indications and uses

Uses spray to reduce bacteria on the skin.

Dosage and administration

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.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Didecyldimethyl Ammonium 0.3%

Triclosan 0.3%

Borneol 0.4%

Benzalkonium Bromide 0.3%

PURPOSES

OTC - PURPOSE SECTION

Antibacterial

KEEP OUT OF REACH OF CHILDREN.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DO NOT USE

OTC - DO NOT USE SECTION

if you are allergic to any of the ingredients.

WHEN USING THIS DEVICE

OTC - WHEN USING SECTION

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

STOP USE AND ASK A DOCTOR IF

OTC - STOP USE SECTION

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

USES

INDICATIONS & USAGE SECTION

Uses spray to reduce bacteria on the skin.

WARNINGS

WARNINGS SECTION

For external use only.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

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

INACTIVE INGREDIENT SECTION

Polyethylene Glycol, Menthol, Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

carton.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
58686-013-01	2019-11-27	C162847	48780-1	9855d018-ea5c-cd31-e053-dbdaa90ab51a	SHUNFA ANTI-BACTERIA SPRAY
58686-013-02	2019-11-27	C162847	48780-1	9855d018-ea5c-cd31-e053-dbdaa90ab51a	SHUNFA ANTI-BACTERIA SPRAY

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
58686-013-01	Shunfa Anti-Bacteria Spra	30 mg in 1 BOTTLE, SPRAY	SPRAY	30		2930
58686-013-02	Shunfa Anti-Bacteria Spra	5 mg in 1 BOTTLE, SPRAY	SPRAY	5		2930

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
58686-013	SHUNFA ANTI-BACTERIA SPRA (DIDECYLDIMETHYL AMMONIUM,TRICLOSAN, BORNEOL, BENZALKONIUM BROMIDE) SPRAY [CHENGDU SHUNFA DISINFECTION AND WASHING TECHNOLOGY CO LTD]	2930	Legacy NDC, 2 package rows	20130606_92cf6f49-d10b-49da-9d36-0aaef95ad6c2.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
BENZALKONIUM BROMIDE	ACTIVE INGREDIENT	151T1GQ42D	2930
BORNEOL	ACTIVE INGREDIENT	M89NIB437X	2930
DIDECYLDIMETHYLAMMONIUM	ACTIVE INGREDIENT	Z7F472XQPA	2930
TRICLOSAN	ACTIVE INGREDIENT	4NM5039Y5X	2930
BENZALKONIUM BROMIDE	ACTIVE MOIETY	151T1GQ42D	2930
BORNEOL	ACTIVE MOIETY	M89NIB437X	2930
DIDECYLDIMETHYLAMMONIUM	ACTIVE MOIETY	Z7F472XQPA	2930
TRICLOSAN	ACTIVE MOIETY	4NM5039Y5X	2930
MENTHOL	INACTIVE INGREDIENT	L7T10EIP3A	2930
POLYETHYLENE GLYCOL 1000	INACTIVE INGREDIENT	U076Q6Q621	2930
WATER	INACTIVE INGREDIENT	059QF0KO0R	2930

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 9 matching rows.

Shunfa Anti-Bacteria Spra
Didecyldimethyl Ammonium,Triclosan, Borneol, Benzalkonium Bromide
DIDECYLDIMETHYLAMMONIUM
TRICLOSAN
BENZALKONIUM BROMIDE
BORNEOL
POLYETHYLENE GLYCOL 1000
MENTHOL
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
58686-013	58686-013-01, 58686-013-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
DIDECYLDIMETHYLAMMONIUM	Z7F472XQPA	ACTIB
TRICLOSAN	4NM5039Y5X	ACTIB
BENZALKONIUM BROMIDE	151T1GQ42D	ACTIB
BORNEOL	M89NIB437X	ACTIB
POLYETHYLENE GLYCOL 1000	U076Q6Q621	IACT
MENTHOL	L7T10EIP3A	IACT
WATER	059QF0KO0R	IACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 33 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Potency	Maximum daily exposure	Match
MENTHOL	MENTHOL	L7T10EIP3A	CAPSULE / ORAL	0.87 mg		Exact identifier — unii candidate 24 equally ranked IID candidates
MENTHOL	MENTHOL	L7T10EIP3A	SYRUP / ORAL	7.5 mg/5ml		Exact identifier — unii candidate 24 equally ranked IID candidates
MENTHOL	MENTHOL	L7T10EIP3A	POWDER, FOR SOLUTION / ORAL	NA		Exact identifier — unii candidate 24 equally ranked IID candidates
MENTHOL	MENTHOL	L7T10EIP3A	AEROSOL, SPRAY / RESPIRATORY (INHALATION)	0.02 %w/w		Exact identifier — unii candidate 24 equally ranked IID candidates
MENTHOL	MENTHOL	L7T10EIP3A	SOAP / TOPICAL	0.75 %w/w		Exact identifier — unii candidate 24 equally ranked IID candidates
MENTHOL	MENTHOL	L7T10EIP3A	DROPS / OPHTHALMIC	NA		Exact identifier — unii candidate 24 equally ranked IID candidates
POLYETHYLENE GLYCOL 1000	POLYETHYLENE GLYCOL 1000	U076Q6Q621	CREAM / TOPICAL	0.5 %w/w		Exact identifier — unii candidate 9 equally ranked IID candidates
MENTHOL	MENTHOL	L7T10EIP3A	INHALANT / NASAL	32 mg		Exact identifier — unii candidate 24 equally ranked IID candidates
MENTHOL	MENTHOL	L7T10EIP3A	CREAM / TOPICAL	0.1 %w/w		Exact identifier — unii candidate 24 equally ranked IID candidates
MENTHOL	MENTHOL	L7T10EIP3A	CONCENTRATE / ORAL	0.05 mg/5ml		Exact identifier — unii candidate 24 equally ranked IID candidates
POLYETHYLENE GLYCOL 1000	POLYETHYLENE GLYCOL 1000	U076Q6Q621	CONCENTRATE / ORAL	100 mg/1ml		Exact identifier — unii candidate 9 equally ranked IID candidates
MENTHOL	MENTHOL	L7T10EIP3A	SOLUTION, CONCENTRATE / ORAL	0.5 mg/1ml		Exact identifier — unii candidate 24 equally ranked IID candidates
POLYETHYLENE GLYCOL 1000	POLYETHYLENE GLYCOL 1000	U076Q6Q621	SUPPOSITORY / RECTAL	1658 mg		Exact identifier — unii candidate 9 equally ranked IID candidates
MENTHOL	MENTHOL	L7T10EIP3A	SUSPENSION / ORAL		1 mg	Exact identifier — unii candidate 24 equally ranked IID candidates
POLYETHYLENE GLYCOL 1000	POLYETHYLENE GLYCOL 1000	U076Q6Q621	AEROSOL, FOAM / TOPICAL	NA		Exact identifier — unii candidate 9 equally ranked IID candidates
MENTHOL	MENTHOL	L7T10EIP3A	PASTE, DENTIFRICE / DENTAL	4.7 %w/w		Exact identifier — unii candidate 24 equally ranked IID candidates
MENTHOL	MENTHOL	L7T10EIP3A	SOLUTION / ORAL		3 mg	Exact identifier — unii candidate 24 equally ranked IID candidates
POLYETHYLENE GLYCOL 1000	POLYETHYLENE GLYCOL 1000	U076Q6Q621	SOLUTION / ORAL	1000 mg/5ml		Exact identifier — unii candidate 9 equally ranked IID candidates
MENTHOL	MENTHOL	L7T10EIP3A	DROPS / NASAL	40.32 mg		Exact identifier — unii candidate 24 equally ranked IID candidates
POLYETHYLENE GLYCOL 1000	POLYETHYLENE GLYCOL 1000	U076Q6Q621	TABLET, FILM COATED / ORAL	1.52 mg		Exact identifier — unii candidate 9 equally ranked IID candidates
MENTHOL	MENTHOL	L7T10EIP3A	TABLET / ORAL	0.58 mg		Exact identifier — unii candidate 24 equally ranked IID candidates
POLYETHYLENE GLYCOL 1000	POLYETHYLENE GLYCOL 1000	U076Q6Q621	GEL / TOPICAL		50 mg	Exact identifier — unii candidate 9 equally ranked IID candidates
POLYETHYLENE GLYCOL 1000	POLYETHYLENE GLYCOL 1000	U076Q6Q621	GEL / TRANSDERMAL	0.5 %w/w		Exact identifier — unii candidate 9 equally ranked IID candidates
MENTHOL	MENTHOL	L7T10EIP3A	TABLET / SUBLINGUAL		2 mg	Exact identifier — unii candidate 24 equally ranked IID candidates
MENTHOL	MENTHOL	L7T10EIP3A	TABLET, ORALLY DISINTEGRATING / ORAL	14 mg		Exact identifier — unii candidate 24 equally ranked IID candidates
MENTHOL	MENTHOL	L7T10EIP3A	GEL / TOPICAL	0.1 %w/w		Exact identifier — unii candidate 24 equally ranked IID candidates
MENTHOL	MENTHOL	L7T10EIP3A	MOUTHWASH / BUCCAL	0.15 mg/1ml		Exact identifier — unii candidate 24 equally ranked IID candidates
POLYETHYLENE GLYCOL 1000	POLYETHYLENE GLYCOL 1000	U076Q6Q621	SUPPOSITORY / VAGINAL	NA		Exact identifier — unii candidate 9 equally ranked IID candidates
MENTHOL	MENTHOL	L7T10EIP3A	SOLUTION / DENTAL	NA		Exact identifier — unii candidate 24 equally ranked IID candidates
MENTHOL	MENTHOL	L7T10EIP3A	GUM, CHEWING / BUCCAL		89 mg	Exact identifier — unii candidate 24 equally ranked IID candidates
MENTHOL	MENTHOL	L7T10EIP3A	JELLY / NASAL	32.5 mg		Exact identifier — unii candidate 24 equally ranked IID candidates
MENTHOL	MENTHOL	L7T10EIP3A	LOTION / TOPICAL	0.05 %w/w		Exact identifier — unii candidate 24 equally ranked IID candidates
MENTHOL	MENTHOL	L7T10EIP3A	AEROSOL, METERED / RESPIRATORY (INHALATION)	0.02 %w/w		Exact identifier — unii candidate 24 equally ranked IID candidates

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
a12a1bd5-c7b7-400f-a8f3-7c7350b61edd			92cf6f49-d10b-49da-9d36-0aaef95ad6c2	2013-06-05	Warnings	Exact identifier spl id: a12a1bd5-c7b7-400f-a8f3-7c7350b61edd spl set id: 92cf6f49-d10b-49da-9d36-0aaef95ad6c2

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.