Supergoop - 75936-118-01 - (Avobenzone, Octinoxate, Octisalate)

Alphabetical Index


Drug Information of Supergoop

Product NDC: 75936-118
Proprietary Name: Supergoop
Non Proprietary Name: Avobenzone, Octinoxate, Octisalate
Active Ingredient(s): .44; 1.11; .74    mL/14.79mL; mL/14.79mL; mL/14.79mL & nbsp;   Avobenzone, Octinoxate, Octisalate
Administration Route(s): TOPICAL
Dosage Form(s): OINTMENT
Coding System: National Drug Codes(NDC)

Labeler Information of Supergoop

Product NDC: 75936-118
Labeler Name: TAYLOR JAMES, LTD.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20120628

Package Information of Supergoop

Package NDC: 75936-118-01
Package Description: 14.79 mL in 1 TUBE (75936-118-01)

NDC Information of Supergoop

NDC Code 75936-118-01
Proprietary Name Supergoop
Package Description 14.79 mL in 1 TUBE (75936-118-01)
Product NDC 75936-118
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Avobenzone, Octinoxate, Octisalate
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 20120628
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name TAYLOR JAMES, LTD.
Substance Name AVOBENZONE; OCTINOXATE; OCTISALATE
Strength Number .44; 1.11; .74
Strength Unit mL/14.79mL; mL/14.79mL; mL/14.79mL
Pharmaceutical Classes

Complete Information of Supergoop


General Information