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SUPER DEFENSE - 49527-708-01 - (OXYBENZONE, OCTISALATE, AVOBENZONE)

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Drug Information of SUPER DEFENSE

Product NDC: 49527-708
Proprietary Name: SUPER DEFENSE
Non Proprietary Name: OXYBENZONE, OCTISALATE, AVOBENZONE
Active Ingredient(s): 3; 5; 5    mL/100mL; mL/100mL; mL/100mL & nbsp;   OXYBENZONE, OCTISALATE, AVOBENZONE
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of SUPER DEFENSE

Product NDC: 49527-708
Labeler Name: CLINIQUE LABORATORIES INC
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20080401

Package Information of SUPER DEFENSE

Package NDC: 49527-708-01
Package Description: 1 JAR in 1 CARTON (49527-708-01) > 50 mL in 1 JAR (49527-708-02)

NDC Information of SUPER DEFENSE

NDC Code 49527-708-01
Proprietary Name SUPER DEFENSE
Package Description 1 JAR in 1 CARTON (49527-708-01) > 50 mL in 1 JAR (49527-708-02)
Product NDC 49527-708
Product Type Name HUMAN OTC DRUG
Non Proprietary Name OXYBENZONE, OCTISALATE, AVOBENZONE
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20080401
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name CLINIQUE LABORATORIES INC
Substance Name AVOBENZONE; OCTISALATE; OXYBENZONE
Strength Number 3; 5; 5
Strength Unit mL/100mL; mL/100mL; mL/100mL
Pharmaceutical Classes

Complete Information of SUPER DEFENSE


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