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"50555-220-02" National Drug Code (NDC)

Foamgle Foam Super Mint 1 BOTTLE in 1 CARTON (50555-220-02) / 150 mL in 1 BOTTLE (50555-220-01)
(KMPHARMACEUTICAL CO.,LTD)

NDC Code50555-220-02
Package Description1 BOTTLE in 1 CARTON (50555-220-02) / 150 mL in 1 BOTTLE (50555-220-01)
Product NDC50555-220
Product Type NameHUMAN OTC DRUG
Proprietary NameFoamgle Foam Super Mint
Non-Proprietary NameAllantoin
Dosage FormMOUTHWASH
UsageORAL
Start Marketing Date20260201
Marketing Category NameUNAPPROVED DRUG OTHER
ManufacturerKMPHARMACEUTICAL CO.,LTD
Substance NameALLANTOIN
Strength.05
Strength Unitg/100mL

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/50555-220-02





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