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Cellular Radiance Emulsion SPF 30 - 76157-302-11 - (Avobenzone, Octinoxate, Octisalate)

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Drug Information of Cellular Radiance Emulsion SPF 30

Product NDC: 76157-302
Proprietary Name: Cellular Radiance Emulsion SPF 30
Non Proprietary Name: Avobenzone, Octinoxate, Octisalate
Active Ingredient(s): 75; 50; 30    mg/mL; mg/mL; mg/mL & nbsp;   Avobenzone, Octinoxate, Octisalate
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Cellular Radiance Emulsion SPF 30

Product NDC: 76157-302
Labeler Name: La Prairie Group AG
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20130111

Package Information of Cellular Radiance Emulsion SPF 30

Package NDC: 76157-302-11
Package Description: 78400 mL in 1 DRUM (76157-302-11)

NDC Information of Cellular Radiance Emulsion SPF 30

NDC Code 76157-302-11
Proprietary Name Cellular Radiance Emulsion SPF 30
Package Description 78400 mL in 1 DRUM (76157-302-11)
Product NDC 76157-302
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Avobenzone, Octinoxate, Octisalate
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20130111
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name La Prairie Group AG
Substance Name AVOBENZONE; OCTINOXATE; OCTISALATE
Strength Number 75; 50; 30
Strength Unit mg/mL; mg/mL; mg/mL
Pharmaceutical Classes

Complete Information of Cellular Radiance Emulsion SPF 30


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