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Cellular Anti-wrinkle Sun SPF 30
Cellular Anti-wrinkle Sun SPF 30 - 68026-414-50 - (AVOBENZONE, OCTINOXATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE)
Drug Information of Cellular Anti-wrinkle Sun SPF 30
| Product NDC: | 68026-414 |
| Proprietary Name: | Cellular Anti-wrinkle Sun SPF 30 |
| Non Proprietary Name: | AVOBENZONE, OCTINOXATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE |
| Active Ingredient(s): | 30; 75; 26; 24; 50 mg/mL; mg/mL; mg/mL; mg/mL; mg/mL & nbsp; AVOBENZONE, OCTINOXATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cellular Anti-wrinkle Sun SPF 30
| Product NDC: | 68026-414 |
| Labeler Name: | La Prairie, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110411 |
Package Information of Cellular Anti-wrinkle Sun SPF 30
| Package NDC: | 68026-414-50 |
| Package Description: | 50 mL in 1 BOTTLE (68026-414-50) |
NDC Information of Cellular Anti-wrinkle Sun SPF 30
| NDC Code | 68026-414-50 |
| Proprietary Name | Cellular Anti-wrinkle Sun SPF 30 |
| Package Description | 50 mL in 1 BOTTLE (68026-414-50) |
| Product NDC | 68026-414 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | AVOBENZONE, OCTINOXATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20110411 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | La Prairie, Inc. |
| Substance Name | AVOBENZONE; OCTINOXATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
| Strength Number | 30; 75; 26; 24; 50 |
| Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |
