"11523-0635-2" National Drug Code (NDC)

Duofilm Wart Remover 1 BOTTLE, WITH APPLICATOR in 1 CARTON (11523-0635-2) > 9.8 mL in 1 BOTTLE, WITH APPLICATOR
(Bayer HealthCare LLC)

NDC Code11523-0635-2
Package Description1 BOTTLE, WITH APPLICATOR in 1 CARTON (11523-0635-2) > 9.8 mL in 1 BOTTLE, WITH APPLICATOR
Product NDC11523-0635
Product Type NameHUMAN OTC DRUG
Proprietary NameDuofilm Wart Remover
Non-Proprietary NameSalicylic Acid
Dosage FormLIQUID
UsageTOPICAL
Start Marketing Date19900814
End Marketing Date20210228
Marketing Category NameOTC MONOGRAPH FINAL
Application Numberpart358B
ManufacturerBayer HealthCare LLC
Substance NameSALICYLIC ACID
Strength150.28
Strength Unitmg/mL

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