ANTI-BACTERIAL CREAM- RHINITIS OINTMENT cream

Anti-bacterial Cream (Rhinitis Ointment) by

Drug Labeling and Warnings

Anti-bacterial Cream (Rhinitis Ointment) by is a Otc medication manufactured, distributed, or labeled by Dongguan Haiyi Technology Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Sophora Flavescens
Radix Stemonae
Fructus Cnidii
Fructus Kochiae Menthol
Chlorhexidine Acetate

Inactive ingredient

Vaseline
Propylene Glycol
Ice Chips

Purpose section

it has inhibitory effect on Staphylococcus aureus,Escherichia coli and Candida albicans.

Warning

1. This product is for extemal use only and is prohibited for oral use

2.Pregnant women and those allergic to this product are prohibited, no adverse reactions have been found.

3.Please keep out of the reach of children.
4.This product is not a substitute for medicine.

stop use

This product may cause allergic reactions in asmall number of people.
lf youexperience any discomfort,please stop using it immediately.

not use

Not suitable for use by children, pregnantor breastfeeding people.

OUT OF CHILDREN

KEEP THE PRODUCT OUT OF REACH OF CHILDREN to

HOW TO USE

Apply an appropriate amount of cream to the skin surface and massage repeatedly to absorb

Dosage

take an appropriateamount,Use 2-3 times a week

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ANTI-BACTERIAL CREAM (RHINITIS OINTMENT) 
anti-bacterial cream (rhinitis ointment) cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84732-022
Route of Administration	INTRASINAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SOPHORA FLAVESCENS WHOLE (UNII: X8KX602M5L) (SOPHORA FLAVESCENS WHOLE - UNII:X8KX602M5L)	SOPHORA FLAVESCENS WHOLE	1 mg  in 10 g
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	1 mg  in 10 g

Inactive Ingredients
Ingredient Name	Strength
CHLORHEXIDINE ACETATE (UNII: 5908ZUF22Y)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84732-022-01	10 g in 1 CAN; Type 0: Not a Combination Product	09/28/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M012	09/28/2024

Labeler - Dongguan Haiyi Technology Co.,Ltd. (722030807)

Establishment
Name	Address	ID/FEI	Business Operations
Dongguan Haiyi Technology Co.,Ltd.		722030807	manufacture(84732-022)