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Ultra Light Sunscreen Broad Spectrum SPF 50 - 57627-117-02 - (Avobenzone, Homosalate, Octisalate, Octocrylene, Oxybenzone)

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Drug Information of Ultra Light Sunscreen Broad Spectrum SPF 50

Product NDC: 57627-117
Proprietary Name: Ultra Light Sunscreen Broad Spectrum SPF 50
Non Proprietary Name: Avobenzone, Homosalate, Octisalate, Octocrylene, Oxybenzone
Active Ingredient(s): 3.39; 11.3; 5.65; 3.11; 6.78    g/113g; g/113g; g/113g; g/113g; g/113g & nbsp;   Avobenzone, Homosalate, Octisalate, Octocrylene, Oxybenzone
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of Ultra Light Sunscreen Broad Spectrum SPF 50

Product NDC: 57627-117
Labeler Name: Merle Norman Cosmetics
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20130329

Package Information of Ultra Light Sunscreen Broad Spectrum SPF 50

Package NDC: 57627-117-02
Package Description: 1 TUBE in 1 CARTON (57627-117-02) > 113 g in 1 TUBE (57627-117-01)

NDC Information of Ultra Light Sunscreen Broad Spectrum SPF 50

NDC Code 57627-117-02
Proprietary Name Ultra Light Sunscreen Broad Spectrum SPF 50
Package Description 1 TUBE in 1 CARTON (57627-117-02) > 113 g in 1 TUBE (57627-117-01)
Product NDC 57627-117
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Avobenzone, Homosalate, Octisalate, Octocrylene, Oxybenzone
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20130329
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Merle Norman Cosmetics
Substance Name AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE
Strength Number 3.39; 11.3; 5.65; 3.11; 6.78
Strength Unit g/113g; g/113g; g/113g; g/113g; g/113g
Pharmaceutical Classes

Complete Information of Ultra Light Sunscreen Broad Spectrum SPF 50


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