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"51206-308-06" National Drug Code (NDC)

Opalescence Sensitivity Relief Whitening 6 CARTON in 1 PACKAGE, COMBINATION (51206-308-06) / 1 TUBE in 1 CARTON / 133 g in 1 TUBE
(Ultradent Products, Inc.)

NDC Code51206-308-06
Package Description6 CARTON in 1 PACKAGE, COMBINATION (51206-308-06) / 1 TUBE in 1 CARTON / 133 g in 1 TUBE
Product NDC51206-308
Product Type NameHUMAN OTC DRUG
Proprietary NameOpalescence Sensitivity Relief Whitening
Non-Proprietary NamePotassium Nitrate And Sodium Fluoride
Dosage FormGEL, DENTIFRICE
UsageDENTAL
Start Marketing Date20151130
Marketing Category NameOTC MONOGRAPH DRUG
Application NumberM022
ManufacturerUltradent Products, Inc.
Substance NamePOTASSIUM NITRATE; SODIUM FLUORIDE
Strength50; 1.1
Strength Unitmg/g; mg/g

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/51206-308-06





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