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Sun Essential - 35192-009-05 - (Octinoxate Titanium Dioxide)

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Drug Information of Sun Essential

Product NDC: 35192-009
Proprietary Name: Sun Essential
Non Proprietary Name: Octinoxate Titanium Dioxide
Active Ingredient(s): 1.5; 1.2    g/30g; g/30g & nbsp;   Octinoxate Titanium Dioxide
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of Sun Essential

Product NDC: 35192-009
Labeler Name: CA-BOTANA INTERNATIONAL
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20120601

Package Information of Sun Essential

Package NDC: 35192-009-05
Package Description: 30 g in 1 TUBE (35192-009-05)

NDC Information of Sun Essential

NDC Code 35192-009-05
Proprietary Name Sun Essential
Package Description 30 g in 1 TUBE (35192-009-05)
Product NDC 35192-009
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Octinoxate Titanium Dioxide
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20120601
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name CA-BOTANA INTERNATIONAL
Substance Name OCTINOXATE; TITANIUM DIOXIDE
Strength Number 1.5; 1.2
Strength Unit g/30g; g/30g
Pharmaceutical Classes

Complete Information of Sun Essential


General Information