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Lubriderm Daily
Lubriderm Daily - 58232-0718-1 - (Avobenzone, Octisalate, Octocrylene, and Oxybenzone)
Drug Information of Lubriderm Daily
| Product NDC: | 58232-0718 |
| Proprietary Name: | Lubriderm Daily |
| Non Proprietary Name: | Avobenzone, Octisalate, Octocrylene, and Oxybenzone |
| Active Ingredient(s): | 20; 40; 30; 22 mg/mL; mg/mL; mg/mL; mg/mL & nbsp; Avobenzone, Octisalate, Octocrylene, and Oxybenzone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Lubriderm Daily
| Product NDC: | 58232-0718 |
| Labeler Name: | Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100601 |
Package Information of Lubriderm Daily
| Package NDC: | 58232-0718-1 |
| Package Description: | 400 mL in 1 BOTTLE, PLASTIC (58232-0718-1) |
NDC Information of Lubriderm Daily
| NDC Code | 58232-0718-1 |
| Proprietary Name | Lubriderm Daily |
| Package Description | 400 mL in 1 BOTTLE, PLASTIC (58232-0718-1) |
| Product NDC | 58232-0718 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Avobenzone, Octisalate, Octocrylene, and Oxybenzone |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20100601 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc. |
| Substance Name | AVOBENZONE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
| Strength Number | 20; 40; 30; 22 |
| Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |
