"58232-0718-1" National Drug Code (NDC)

Lubriderm Daily 400 mL in 1 BOTTLE, PLASTIC (58232-0718-1)
(Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc.)

NDC Code58232-0718-1
Package Description400 mL in 1 BOTTLE, PLASTIC (58232-0718-1)
Product NDC58232-0718
Product Type NameHUMAN OTC DRUG
Proprietary NameLubriderm Daily
Proprietary Name SuffixMoisturizer With Sunscreen Spf15
Non-Proprietary NameAvobenzone, Octisalate, Octocrylene, And Oxybenzone
Dosage FormLOTION
UsageTOPICAL
Start Marketing Date20100601
End Marketing Date20150601
Marketing Category NameOTC MONOGRAPH FINAL
Application Numberpart352
ManufacturerJohnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc.
Substance NameAVOBENZONE; OCTISALATE; OCTOCRYLENE; OXYBENZONE
Strength20; 40; 30; 22
Strength Unitmg/mL; mg/mL; mg/mL; mg/mL

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