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"58443-0129-4" National Drug Code (NDC)

Ulta 177 mL in 1 TUBE (58443-0129-4)
(Prime Enterprises, Inc.)

NDC Code58443-0129-4
Package Description177 mL in 1 TUBE (58443-0129-4)
Product NDC58443-0129
Product Type NameHUMAN OTC DRUG
Proprietary NameUlta
Proprietary Name SuffixSunscreen Spf 45
Non-Proprietary NameOctinoxate, Octisalate, Octocrylene, And Oxybenzone
Dosage FormLOTION
UsageTOPICAL
Start Marketing Date20070312
Marketing Category NameOTC MONOGRAPH FINAL
Application Numberpart352
ManufacturerPrime Enterprises, Inc.
Substance NameOCTINOXATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE
Strength71.25; 47.5; 76; 57
Strength Unitmg/mL; mg/mL; mg/mL; mg/mL

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/58443-0129-4





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