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"58443-0131-4" National Drug Code (NDC)

Ulta 177 mL in 1 TUBE (58443-0131-4)
(Prime Enterprises, Inc.)

NDC Code58443-0131-4
Package Description177 mL in 1 TUBE (58443-0131-4)
Product NDC58443-0131
Product Type NameHUMAN OTC DRUG
Proprietary NameUlta
Proprietary Name SuffixSpf 15 Medium Deep Broad Spectrum Tinted Sunscreen
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
Strength19.6; 49; 18.13
Strength Unitmg/mL; mg/mL; mg/mL

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/58443-0131-4





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