Cygzyme by Valley Inc.

Cygzyme by

Drug Labeling and Warnings

Cygzyme by is a Otc medication manufactured, distributed, or labeled by Valley Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

CYGZYME- citric acid liquid 
Valley Inc.

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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ACTIVE INGREDIENT

CITRIC ACID 4.0%

INACTIVE INGREDIENTS

Water, Sodium hydrogencarbonate, Gluconic acid, Sodium salt, N-Ethylenediaminediacetic acid,Dihydrogen Oxide

PURPOSE

Antifungal

WARNINGS

For external use only
Do not use on the human body
Avoid contact with eyes.
Discontinue use if signs of irritation or rashes appear.
Keep out of reach of children

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children

Uses

Helps prevent sterilant

Directions

■Rinse thoroughly for more than 5 minutes. Rinse for more than 15 seconds with sterile purified water flowing out after soaking.
■After the disinfection of the medical instrument is completed, confirm the persistence.
■Excess water may be used depending on the purpose of use.

QUESTIONS

+82 02 1566 2723

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CYGZYME 
citric acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81803-040
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) (ANHYDROUS CITRIC ACID - UNII:XF417D3PSL)	ANHYDROUS CITRIC ACID	160.0 g  in 4000 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
GLUCONIC ACID (UNII: R4R8J0Q44B)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81803-040-02	1 in 1 CARTON	05/01/2022	12/01/2022
1	NDC: 81803-040-01	4000 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		05/01/2022	12/01/2022

Labeler - Valley Inc. (695095445)

Registrant - Valley Inc. (695095445)

Establishment
Name	Address	ID/FEI	Business Operations
Valley Inc.		695095445	manufacture(81803-040)

Revised: 3/2024

Document Id: 10dd95c1-ffe0-43e0-bbf2-9b6ca4e0d990

34390-5

Set id: c1b0c21f-0b9a-4586-ac5c-02daa690249a

Version: 2

Effective Time: 20240312