DR.VIR GERM PEROYXACETIC ACID MULTI-DISINFECTANT- peroxyacetic acid liquid

Dr.Vir Germ Peroyxacetic acid Multi-disinfectant by

Drug Labeling and Warnings

Dr.Vir Germ Peroyxacetic acid Multi-disinfectant by is a Otc medication manufactured, distributed, or labeled by JANGIN PHARM CO.,LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

alcohol, Peroxyacetic acid

INACTIVE INGREDIENT

Water, Surfactants : Polyoxyethylene alkyl ether (nonionic)

PURPOSE

multi disinfectant

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children

INDICATIONS & USAGE

1. Sprinkle 20 cm away until moist 2.It is more effective if sprayed repeatedly every day.[Storage precautions] Store at room temperature(1-30 degrees Celsius) [labeling items of household chemicals subject to safety verification]

WARNINGS

1. When it gets into your eyes, do not rub them, immediately wash them with clean water, and if there is any abnormality, consult a doctor.

2. Do not drink it, or if you drink it, take measures such as drinking water or milk, and

then consult a doctor.

3. Do not use for any purpose other than

4. Do not spray directly on humans or food

5. Do not mix with other products.

6. Do not place in direct sunlight or in high temperature.

DOSAGE & ADMINISTRATION

for external use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DR.VIR GERM PEROYXACETIC ACID MULTI-DISINFECTANT 
peroxyacetic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69255-600
Route of Administration	DENTAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PERACETIC ACID (UNII: I6KPI2E1HD) (PERACETIC ACID - UNII:I6KPI2E1HD)	PERACETIC ACID	5 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
PAEONIA LACTIFLORA ROOT OIL (UNII: BC82X683T4)
WATER (UNII: 059QF0KO0R)
CULTIVATED MUSHROOM (UNII: 54C8E6W6JY)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
LEVOMENTHOL (UNII: BZ1R15MTK7)
ALCOHOL (UNII: 3K9958V90M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69255-600-01	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/26/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		05/26/2020

Labeler - JANGIN PHARM CO.,LTD. (688733680)

Registrant - JANGIN PHARM CO.,LTD. (688733680)

Establishment
Name	Address	ID/FEI	Business Operations
JANGIN PHARM CO.,LTD.		688733680	manufacture(69255-600)