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