BACTERIA ZERO PREMIUM- peracetic acid liquid

BACTERIA ZERO PREMIUM by

Drug Labeling and Warnings

BACTERIA ZERO PREMIUM by is a Otc medication manufactured, distributed, or labeled by KUMSUNG E&C CO., LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient[s]

Peracetic acid 0.015%

Purpose

Antiseptic

USE[s]

Fruits, Vegetables, Meat Sterilization(Food Additives), General Object surface Sterilization
Sanitizer to help reduce bacteria that potentially can disease.

WARNINGS

For external use only. Flammable. Keep away form heat or flame
Check the indications before use.
Do not inhale the contents that are sprayed or sprayed directly on a person.

When using this product

keep away from eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor

if irritation or rash occurs. These may be signs of a serious condition

Keep out of reach of children.

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

DIRECTIONS

- If the original solution is sprayed on a contaminated place, wipe it with a dry cloth or if it is naturally dried, harmful bacteria are immediately sterilized.
- Supervise children under 6 years of age when using this product to avoid swallowing.

OTHER INFORMATION

- Store between 1~30℃(33.8~86℉)
- Avoid freezing(-5℃) and excessive heat above 35℃(86℉)

INACTIVE INGREDIENTS

acetic acid, hydrogen peroxide, Phosphonic acid, purified water USP

Package Label

INGREDIENTS AND APPEARANCE

BACTERIA ZERO PREMIUM 
peracetic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80138-204
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PERACETIC ACID (UNII: I6KPI2E1HD) (PERACETIC ACID - UNII:I6KPI2E1HD)	PERACETIC ACID	0.015 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
PHOSPHOROUS ACID (UNII: 35V6A8JW8E)
HYDROGEN PEROXIDE (UNII: BBX060AN9V)
WATER (UNII: 059QF0KO0R)
ACETIC ACID (UNII: Q40Q9N063P)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80138-204-01	60 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	01/01/2022
2	NDC: 80138-204-02	500 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	01/01/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		01/01/2022

Labeler - KUMSUNG E&C CO., LTD (688082226)

Registrant - KUMSUNG E&C CO., LTD (688082226)

Establishment
Name	Address	ID/FEI	Business Operations
KUMSUNG E&C CO., LTD		688082226	manufacture(80138-204)