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OBAGI-C RX SYSTEM C-EXFOLIATING DAY - 62032-108-36 - (OCTISALATE, OCTINOXATE, and OXYBENZONE)

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Drug Information of OBAGI-C RX SYSTEM C-EXFOLIATING DAY

Product NDC: 62032-108
Proprietary Name: OBAGI-C RX SYSTEM C-EXFOLIATING DAY
Non Proprietary Name: OCTISALATE, OCTINOXATE, and OXYBENZONE
Active Ingredient(s): 75; 50; 40    mg/mL; mg/mL; mg/mL & nbsp;   OCTISALATE, OCTINOXATE, and OXYBENZONE
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of OBAGI-C RX SYSTEM C-EXFOLIATING DAY

Product NDC: 62032-108
Labeler Name: OMP, INC.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20040101

Package Information of OBAGI-C RX SYSTEM C-EXFOLIATING DAY

Package NDC: 62032-108-36
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (62032-108-36) > 57 mL in 1 BOTTLE, PLASTIC

NDC Information of OBAGI-C RX SYSTEM C-EXFOLIATING DAY

NDC Code 62032-108-36
Proprietary Name OBAGI-C RX SYSTEM C-EXFOLIATING DAY
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (62032-108-36) > 57 mL in 1 BOTTLE, PLASTIC
Product NDC 62032-108
Product Type Name HUMAN OTC DRUG
Non Proprietary Name OCTISALATE, OCTINOXATE, and OXYBENZONE
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20040101
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name OMP, INC.
Substance Name OCTINOXATE; OCTISALATE; OXYBENZONE
Strength Number 75; 50; 40
Strength Unit mg/mL; mg/mL; mg/mL
Pharmaceutical Classes

Complete Information of OBAGI-C RX SYSTEM C-EXFOLIATING DAY


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