Supergoop - 75936-119-01 - (Octinoxate, Octocrylene, Titanium Dioxide, Zinc Oxide)

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Drug Information of Supergoop

Product NDC: 75936-119
Proprietary Name: Supergoop
Non Proprietary Name: Octinoxate, Octocrylene, Titanium Dioxide, Zinc Oxide
Active Ingredient(s): 5.24; 2.13; 2.34; 14.2    mL/71mL; mL/71mL; mL/71mL; mL/71mL & nbsp;   Octinoxate, Octocrylene, Titanium Dioxide, Zinc Oxide
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Supergoop

Product NDC: 75936-119
Labeler Name: Taylor James Ltd
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20120630

Package Information of Supergoop

Package NDC: 75936-119-01
Package Description: 1 TUBE in 1 BOX (75936-119-01) > 71 mL in 1 TUBE

NDC Information of Supergoop

NDC Code 75936-119-01
Proprietary Name Supergoop
Package Description 1 TUBE in 1 BOX (75936-119-01) > 71 mL in 1 TUBE
Product NDC 75936-119
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Octinoxate, Octocrylene, Titanium Dioxide, Zinc Oxide
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20120630
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Taylor James Ltd
Substance Name OCTINOXATE; OCTOCRYLENE; TITANIUM DIOXIDE; ZINC OXIDE
Strength Number 5.24; 2.13; 2.34; 14.2
Strength Unit mL/71mL; mL/71mL; mL/71mL; mL/71mL
Pharmaceutical Classes

Complete Information of Supergoop


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