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Purpose
Purpose - 58232-9809-1 - (Octinoxate, Octisalate and Oxybenzone)
Drug Information of Purpose
| Product NDC: | 58232-9809 |
| Proprietary Name: | Purpose |
| Non Proprietary Name: | Octinoxate, Octisalate and Oxybenzone |
| Active Ingredient(s): | 76; 50; 30 mg/mL; mg/mL; mg/mL & nbsp; Octinoxate, Octisalate and Oxybenzone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Purpose
| Product NDC: | 58232-9809 |
| 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: | 20091101 |
Package Information of Purpose
| Package NDC: | 58232-9809-1 |
| Package Description: | 1 BOTTLE, PUMP in 1 CARTON (58232-9809-1) > 120 mL in 1 BOTTLE, PUMP |
NDC Information of Purpose
| NDC Code | 58232-9809-1 |
| Proprietary Name | Purpose |
| Package Description | 1 BOTTLE, PUMP in 1 CARTON (58232-9809-1) > 120 mL in 1 BOTTLE, PUMP |
| Product NDC | 58232-9809 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate, Octisalate and Oxybenzone |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20091101 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc. |
| Substance Name | OCTINOXATE; OCTISALATE; OXYBENZONE |
| Strength Number | 76; 50; 30 |
| Strength Unit | mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |
