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"52648-6175-1" National Drug Code (NDC)

Sunscreen Wipe 9 mL in 1 PACKET (52648-6175-1)
(KGP Products, Inc. (dba PREMIER))

NDC Code52648-6175-1
Package Description9 mL in 1 PACKET (52648-6175-1)
Product NDC52648-6175
Product Type NameHUMAN OTC DRUG
Proprietary NameSunscreen Wipe
Proprietary Name SuffixKgp
Non-Proprietary NameHomosalate Octinoxate Octisalate Oxybenzone
Dosage FormCLOTH
UsageTOPICAL
Start Marketing Date20100928
Marketing Category NameOTC MONOGRAPH FINAL
Application Numberpart352
ManufacturerKGP Products, Inc. (dba PREMIER)
Substance NameHOMOSALATE; OCTINOXATE; OCTISALATE; OXYBENZONE
Strength20; 75; 40; 50
Strength Unitg/856mL; g/856mL; g/856mL; g/856mL

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/52648-6175-1





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