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"51206-315-01" National Drug Code (NDC)

Opalescence Whitening Sensitivity Relief 1 TUBE in 1 CARTON (51206-315-01) / 133 g in 1 TUBE
(Ultradent Products, Inc.)

NDC Code51206-315-01
Package Description1 TUBE in 1 CARTON (51206-315-01) / 133 g in 1 TUBE
Product NDC51206-315
Product Type NameHUMAN OTC DRUG
Proprietary NameOpalescence Whitening Sensitivity Relief
Non-Proprietary NamePotassium Nitrate And Sodium Fluoride
Dosage FormGEL, DENTIFRICE
UsageDENTAL
Start Marketing Date20251008
Marketing Category NameOTC MONOGRAPH DRUG
Application NumberM022
ManufacturerUltradent Products, Inc.
Substance NameSODIUM FLUORIDE; POTASSIUM NITRATE
Strength1.1; 50
Strength Unitmg/g; mg/g

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/51206-315-01





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