| Product NDC: | 58232-0333 |
| Proprietary Name: | Clean and Clear |
| Non Proprietary Name: | Avobenzone, Octisalate, Oxybenzone and Octocrylene |
| Active Ingredient(s): | 30; 50; 17; 30 mg/g; mg/g; mg/g; mg/g & nbsp; Avobenzone, Octisalate, Oxybenzone and Octocrylene |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 58232-0333 |
| Labeler Name: | Johnson & Johnson Consumer Products Co., 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: | 20091115 |
| Package NDC: | 58232-0333-1 |
| Package Description: | 14.2 g in 1 PACKET (58232-0333-1) |
| NDC Code | 58232-0333-1 |
| Proprietary Name | Clean and Clear |
| Package Description | 14.2 g in 1 PACKET (58232-0333-1) |
| Product NDC | 58232-0333 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Avobenzone, Octisalate, Oxybenzone and Octocrylene |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20091115 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Johnson & Johnson Consumer Products Co., Division of Johnson & Johnson Consumer Companies, inc. |
| Substance Name | AVOBENZONE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
| Strength Number | 30; 50; 17; 30 |
| Strength Unit | mg/g; mg/g; mg/g; mg/g |
| Pharmaceutical Classes |