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LUBRIDERM
LUBRIDERM - 58232-0748-8 - (Avobenzone, Homosalate, Octisalate, Oxybenzone and Octocrylene)
Drug Information of LUBRIDERM
| Product NDC: | 58232-0748 |
| Proprietary Name: | LUBRIDERM |
| Non Proprietary Name: | Avobenzone, Homosalate, Octisalate, Oxybenzone and Octocrylene |
| Active Ingredient(s): | 30; 60; 50; 35.5; 50 mg/g; mg/g; mg/g; mg/g; mg/g & nbsp; Avobenzone, Homosalate, Octisalate, Oxybenzone and Octocrylene |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of LUBRIDERM
| Product NDC: | 58232-0748 |
| 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 NOT FINAL |
| Start Marketing Date: | 20100330 |
Package Information of LUBRIDERM
| Package NDC: | 58232-0748-8 |
| Package Description: | 227 g in 1 TUBE (58232-0748-8) |
NDC Information of LUBRIDERM
| NDC Code | 58232-0748-8 |
| Proprietary Name | LUBRIDERM |
| Package Description | 227 g in 1 TUBE (58232-0748-8) |
| Product NDC | 58232-0748 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Avobenzone, Homosalate, Octisalate, Oxybenzone and Octocrylene |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20100330 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc. |
| Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
| Strength Number | 30; 60; 50; 35.5; 50 |
| Strength Unit | mg/g; mg/g; mg/g; mg/g; mg/g |
| Pharmaceutical Classes |
