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Sun Protection Emulsion Face Broad Spectrum SPF 30 - 76157-222-02 - (Avobenzone, Homosalate, Octisalate, Octocrylene, Oxybenzone)

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Drug Information of Sun Protection Emulsion Face Broad Spectrum SPF 30

Product NDC: 76157-222
Proprietary Name: Sun Protection Emulsion Face Broad Spectrum SPF 30
Non Proprietary Name: Avobenzone, Homosalate, Octisalate, Octocrylene, Oxybenzone
Active Ingredient(s): 3; 10; 2.6; 2.4; 5    g/100mL; g/100mL; g/100mL; g/100mL; g/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 Broad Spectrum SPF 30

Product NDC: 76157-222
Labeler Name: La Prairie Group AG
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20110214

Package Information of Sun Protection Emulsion Face Broad Spectrum SPF 30

Package NDC: 76157-222-02
Package Description: 1 TUBE in 1 CARTON (76157-222-02) > 125 mL in 1 TUBE (76157-222-01)

NDC Information of Sun Protection Emulsion Face Broad Spectrum SPF 30

NDC Code 76157-222-02
Proprietary Name Sun Protection Emulsion Face Broad Spectrum SPF 30
Package Description 1 TUBE in 1 CARTON (76157-222-02) > 125 mL in 1 TUBE (76157-222-01)
Product NDC 76157-222
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 NOT FINAL
Labeler Name La Prairie Group AG
Substance Name AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE
Strength Number 3; 10; 2.6; 2.4; 5
Strength Unit g/100mL; g/100mL; g/100mL; g/100mL; g/100mL
Pharmaceutical Classes

Complete Information of Sun Protection Emulsion Face Broad Spectrum SPF 30


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