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"52000-112-01" National Drug Code (NDC)

Universal Advanced Whitening Anti-cavity Fluoride 181 g in 1 TUBE (52000-112-01)
(Universal Distribution Center LLC)

NDC Code52000-112-01
Package Description181 g in 1 TUBE (52000-112-01)
Product NDC52000-112
Product Type NameHUMAN OTC DRUG
Proprietary NameUniversal Advanced Whitening Anti-cavity Fluoride
Non-Proprietary NameSodium Monofluorophosphate
Dosage FormPASTE
UsageDENTAL
Start Marketing Date20200530
Marketing Category NameOTC MONOGRAPH DRUG
Application NumberM021
ManufacturerUniversal Distribution Center LLC
Substance NameSODIUM MONOFLUOROPHOSPHATE
Strength.76
Strength Unitg/100g

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/52000-112-01





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