Product NDC: | 58232-0030 |
Proprietary Name: | Clean and Clear |
Non Proprietary Name: | Octinoxate and Titanium Dioxide |
Active Ingredient(s): | 80; 30 mg/g; mg/g & nbsp; Octinoxate and Titanium Dioxide |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 58232-0030 |
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: | 20101201 |
Package NDC: | 58232-0030-2 |
Package Description: | 1 TUBE in 1 CARTON (58232-0030-2) > 48 g in 1 TUBE |
NDC Code | 58232-0030-2 |
Proprietary Name | Clean and Clear |
Package Description | 1 TUBE in 1 CARTON (58232-0030-2) > 48 g in 1 TUBE |
Product NDC | 58232-0030 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Octinoxate and Titanium Dioxide |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20101201 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc. |
Substance Name | OCTINOXATE; TITANIUM DIOXIDE |
Strength Number | 80; 30 |
Strength Unit | mg/g; mg/g |
Pharmaceutical Classes |