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Pro Therapy MD
Pro Therapy MD - 0187-2303-01 - (Homosalate, Octinoxate, Octocrylene, and Zinc oxide)
Drug Information of Pro Therapy MD
| Product NDC: | 0187-2303 |
| Proprietary Name: | Pro Therapy MD |
| Non Proprietary Name: | Homosalate, Octinoxate, Octocrylene, and Zinc oxide |
| Active Ingredient(s): | 12; 7.5; 2; 5 g/100g; g/100g; g/100g; g/100g & nbsp; Homosalate, Octinoxate, Octocrylene, and Zinc oxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Pro Therapy MD
| Product NDC: | 0187-2303 |
| Labeler Name: | Valeant Pharmaceuticals North America LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20111219 |
Package Information of Pro Therapy MD
| Package NDC: | 0187-2303-01 |
| Package Description: | 35 g in 1 BOTTLE, PUMP (0187-2303-01) |
NDC Information of Pro Therapy MD
| NDC Code | 0187-2303-01 |
| Proprietary Name | Pro Therapy MD |
| Package Description | 35 g in 1 BOTTLE, PUMP (0187-2303-01) |
| Product NDC | 0187-2303 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Homosalate, Octinoxate, Octocrylene, and Zinc oxide |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20111219 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Valeant Pharmaceuticals North America LLC |
| Substance Name | HOMOSALATE; OCTINOXATE; OCTOCRYLENE; ZINC OXIDE |
| Strength Number | 12; 7.5; 2; 5 |
| Strength Unit | g/100g; g/100g; g/100g; g/100g |
| Pharmaceutical Classes |
