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"58443-0111-4" National Drug Code (NDC)

Ulta 177 mL in 1 BOTTLE (58443-0111-4)
(Prime Enterprises, Inc.)

NDC Code58443-0111-4
Package Description177 mL in 1 BOTTLE (58443-0111-4)
Product NDC58443-0111
Product Type NameHUMAN OTC DRUG
Proprietary NameUlta
Proprietary Name SuffixOil Free Sunscreen Spf30
Non-Proprietary NameHomosalate, Octinoxate, Octisalate, And Oxybenzone
Dosage FormLOTION
UsageTOPICAL
Start Marketing Date20130423
Marketing Category NameOTC MONOGRAPH FINAL
Application Numberpart352
ManufacturerPrime Enterprises, Inc.
Substance NameHOMOSALATE; OCTINOXATE; OCTISALATE; OXYBENZONE
Strength57; 71.25; 47.5; 38
Strength Unitmg/mL; mg/mL; mg/mL; mg/mL

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/58443-0111-4





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