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Sun Protection Emulsion Face - 59614-221-02 - (Avobenzone, Homosalate, octisalate, octocrylene, oxybenzone)

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Drug Information of Sun Protection Emulsion Face

Product NDC: 59614-221
Proprietary Name: Sun Protection Emulsion Face
Non Proprietary Name: Avobenzone, Homosalate, octisalate, octocrylene, oxybenzone
Active Ingredient(s): 3; 10; 2.5; 2.4; 5    mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp;   Avobenzone, Homosalate, octisalate, octocrylene, oxybenzone
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Sun Protection Emulsion Face

Product NDC: 59614-221
Labeler Name: Juvena GMBH
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20110214

Package Information of Sun Protection Emulsion Face

Package NDC: 59614-221-02
Package Description: 1 BOTTLE in 1 BOX (59614-221-02) > 125 mL in 1 BOTTLE (59614-221-01)

NDC Information of Sun Protection Emulsion Face

NDC Code 59614-221-02
Proprietary Name Sun Protection Emulsion Face
Package Description 1 BOTTLE in 1 BOX (59614-221-02) > 125 mL in 1 BOTTLE (59614-221-01)
Product NDC 59614-221
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Avobenzone, Homosalate, octisalate, octocrylene, oxybenzone
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20110214
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Juvena GMBH
Substance Name AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE
Strength Number 3; 10; 2.5; 2.4; 5
Strength Unit mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL
Pharmaceutical Classes

Complete Information of Sun Protection Emulsion Face


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