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"58443-0132-3" National Drug Code (NDC)

Ulta 118 mL in 1 TUBE (58443-0132-3)
(Prime Enterprises, Inc.)

NDC Code58443-0132-3
Package Description118 mL in 1 TUBE (58443-0132-3)
Product NDC58443-0132
Product Type NameHUMAN OTC DRUG
Proprietary NameUlta
Proprietary Name SuffixSpf 15 Broad Spectrum Tinted Sunless Sunscreen For Face
Non-Proprietary NameAvobenzone, Octisalate, And Octocrylene
Dosage FormLOTION
UsageTOPICAL
Start Marketing Date20131125
Marketing Category NameOTC MONOGRAPH FINAL
Application Numberpart352
ManufacturerPrime Enterprises, Inc.
Substance NameAVOBENZONE; OCTISALATE; OCTOCRYLENE
Strength19.44; 48.6; 17.982
Strength Unitmg/mL; mg/mL; mg/mL

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/58443-0132-3





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