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"68479-213-01" National Drug Code (NDC)

Purelight 10 mL in 1 TUBE (68479-213-01)
(Dermalogica, Inc.)

NDC Code68479-213-01
Package Description10 mL in 1 TUBE (68479-213-01)
Product NDC68479-213
Product Type NameHUMAN OTC DRUG
Proprietary NamePurelight
Proprietary Name SuffixSpf50
Non-Proprietary NameAvobenzone And Octinoxate
Dosage FormLOTION
UsageTOPICAL
Start Marketing Date20140218
Marketing Category NameOTC MONOGRAPH FINAL
Application Numberpart352
ManufacturerDermalogica, Inc.
Substance NameAVOBENZONE; OCTINOXATE
Strength30; 75
Strength Unitmg/mL; mg/mL

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68479-213-01





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