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

Image of cartonImage of carton

CYGZYME 
citric acid liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 81803-040
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) (ANHYDROUS CITRIC ACID - UNII:XF417D3PSL) ANHYDROUS CITRIC ACID160.0 g  in 4000 mL
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
GLUCONIC ACID (UNII: R4R8J0Q44B)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 81803-040-021 in 1 CARTON05/01/202212/01/2022
1NDC: 81803-040-014000 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other05/01/202212/01/2022
Labeler - Valley Inc. (695095445)
Registrant - Valley Inc. (695095445)
Establishment
NameAddressID/FEIBusiness Operations
Valley Inc.695095445manufacture(81803-040)

Revised: 3/2024
 

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