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Skin Active
Skin Active - 49203-710-01 - (Octocrylene, Avobenzone, Oxybenzone, and Ensulizole)
Drug Information of Skin Active
| Product NDC: | 49203-710 |
| Proprietary Name: | Skin Active |
| Non Proprietary Name: | Octocrylene, Avobenzone, Oxybenzone, and Ensulizole |
| Active Ingredient(s): | 19.9; 9.9; 49.7; 9.9 mg/mL; mg/mL; mg/mL; mg/mL & nbsp; Octocrylene, Avobenzone, Oxybenzone, and Ensulizole |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Skin Active
| Product NDC: | 49203-710 |
| Labeler Name: | Cat Media Pty Ltd |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110701 |
Package Information of Skin Active
| Package NDC: | 49203-710-01 |
| Package Description: | 1 BOTTLE, PUMP in 1 CARTON (49203-710-01) > 50 mL in 1 BOTTLE, PUMP |
NDC Information of Skin Active
| NDC Code | 49203-710-01 |
| Proprietary Name | Skin Active |
| Package Description | 1 BOTTLE, PUMP in 1 CARTON (49203-710-01) > 50 mL in 1 BOTTLE, PUMP |
| Product NDC | 49203-710 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octocrylene, Avobenzone, Oxybenzone, and Ensulizole |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20110701 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Cat Media Pty Ltd |
| Substance Name | AVOBENZONE; ENSULIZOLE; OCTOCRYLENE; OXYBENZONE |
| Strength Number | 19.9; 9.9; 49.7; 9.9 |
| Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |
