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Cellular Radiance SPF 30
Cellular Radiance SPF 30 - 68026-650-50 - (OCTINOXATE, OCTISALATE, OXYBENZONE)
Drug Information of Cellular Radiance SPF 30
| Product NDC: | 68026-650 |
| Proprietary Name: | Cellular Radiance SPF 30 |
| Non Proprietary Name: | OCTINOXATE, OCTISALATE, OXYBENZONE |
| Active Ingredient(s): | 7.5; 5; 3 mL/100mL; mL/100mL; mL/100mL & nbsp; OCTINOXATE, OCTISALATE, OXYBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | EMULSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cellular Radiance SPF 30
| Product NDC: | 68026-650 |
| Labeler Name: | La Prairie, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20111010 |
Package Information of Cellular Radiance SPF 30
| Package NDC: | 68026-650-50 |
| Package Description: | 1 JAR in 1 CARTON (68026-650-50) > 50 mL in 1 JAR |
NDC Information of Cellular Radiance SPF 30
| NDC Code | 68026-650-50 |
| Proprietary Name | Cellular Radiance SPF 30 |
| Package Description | 1 JAR in 1 CARTON (68026-650-50) > 50 mL in 1 JAR |
| Product NDC | 68026-650 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, OCTISALATE, OXYBENZONE |
| Dosage Form Name | EMULSION |
| Route Name | TOPICAL |
| Start Marketing Date | 20111010 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | La Prairie, Inc. |
| Substance Name | OCTINOXATE; OCTISALATE; OXYBENZONE |
| Strength Number | 7.5; 5; 3 |
| Strength Unit | mL/100mL; mL/100mL; mL/100mL |
| Pharmaceutical Classes |
