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"71502-001-02" National Drug Code (NDC)

Uniwell Aqua Suncream 1 CONTAINER in 1 CARTON (71502-001-02) > 50 mL in 1 CONTAINER (71502-001-01)
(uniwell LTD)

NDC Code71502-001-02
Package Description1 CONTAINER in 1 CARTON (71502-001-02) > 50 mL in 1 CONTAINER (71502-001-01)
Product NDC71502-001
Product Type NameHUMAN OTC DRUG
Proprietary NameUniwell Aqua Suncream
Non-Proprietary NameOctinoxate, Octisalate
Dosage FormCREAM
UsageTOPICAL
Start Marketing Date20170612
Marketing Category NameOTC MONOGRAPH NOT FINAL
Application Numberpart352
Manufactureruniwell LTD
Substance NameOCTINOXATE; OCTISALATE
Strength3.5; 2.25
Strength Unitmg/50mL; mg/50mL

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/71502-001-02





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