DERMAPROT - 66854-026-03 - (OCTINOXATE,TITANIUM DIOXIDE,OXYBENZONE,AVOBENZONE)

Alphabetical Index


Drug Information of DERMAPROT

Product NDC: 66854-026
Proprietary Name: DERMAPROT
Non Proprietary Name: OCTINOXATE,TITANIUM DIOXIDE,OXYBENZONE,AVOBENZONE
Active Ingredient(s): 2.5; 7.5; 1.5; 3    mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp;   OCTINOXATE,TITANIUM DIOXIDE,OXYBENZONE,AVOBENZONE
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of DERMAPROT

Product NDC: 66854-026
Labeler Name: SPAI-SONS PHARMACEUTICAL INTERNATIONAL COSMETICS
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20120630

Package Information of DERMAPROT

Package NDC: 66854-026-03
Package Description: 70 mL in 1 BOTTLE (66854-026-03)

NDC Information of DERMAPROT

NDC Code 66854-026-03
Proprietary Name DERMAPROT
Package Description 70 mL in 1 BOTTLE (66854-026-03)
Product NDC 66854-026
Product Type Name HUMAN OTC DRUG
Non Proprietary Name OCTINOXATE,TITANIUM DIOXIDE,OXYBENZONE,AVOBENZONE
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20120630
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name SPAI-SONS PHARMACEUTICAL INTERNATIONAL COSMETICS
Substance Name AVOBENZONE; OCTINOXATE; OXYBENZONE; TITANIUM DIOXIDE
Strength Number 2.5; 7.5; 1.5; 3
Strength Unit mL/100mL; mL/100mL; mL/100mL; mL/100mL
Pharmaceutical Classes

Complete Information of DERMAPROT


General Information