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"37000-519-02" National Drug Code (NDC)

Crest Sensitivity 1 TUBE in 1 CARTON (37000-519-02) > 24 g in 1 TUBE (37000-519-01)
(Procter & Gamble Manufacturing Company)

NDC Code37000-519-02
Package Description1 TUBE in 1 CARTON (37000-519-02) > 24 g in 1 TUBE (37000-519-01)
Product NDC37000-519
Product Type NameHUMAN OTC DRUG
Proprietary NameCrest Sensitivity
Proprietary Name SuffixClinical Sensitivity Relief
Non-Proprietary NamePotassium Nitrate And Sodium Fluoride
Dosage FormPASTE, DENTIFRICE
UsageDENTAL
Start Marketing Date20100830
Marketing Category NameOTC MONOGRAPH FINAL
Application Numberpart355
ManufacturerProcter & Gamble Manufacturing Company
Substance NamePOTASSIUM NITRATE; SODIUM FLUORIDE
Strength.05; 243
Strength Unitg/g; g/g

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/37000-519-02





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