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"37000-617-19" National Drug Code (NDC)

Dawn Ultra Antibacterial Hand 192 mL in 1 BOTTLE, PLASTIC (37000-617-19)
(The Procter & Gamble Manufacturing Company)

NDC Code37000-617-19
Package Description192 mL in 1 BOTTLE, PLASTIC (37000-617-19)
Product NDC37000-617
Product Type NameHUMAN OTC DRUG
Proprietary NameDawn Ultra Antibacterial Hand
Proprietary Name SuffixOrange Scent
Non-Proprietary NameChloroxylenol
Dosage FormSOAP
UsageTOPICAL
Start Marketing Date20140707
Marketing Category NameOTC MONOGRAPH DRUG
Application NumberM003
ManufacturerThe Procter & Gamble Manufacturing Company
Substance NameCHLOROXYLENOL
Strength.3
Strength Unitg/100mL

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/37000-617-19





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