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M.D. FORTE Aftercare Environmental Protection Sunscreen SPF 30
M.D. FORTE Aftercare Environmental Protection Sunscreen SPF 30 - 0023-1134-25 - (octinoxate, octisalate, zinc oxide)
Drug Information of M.D. FORTE Aftercare Environmental Protection Sunscreen SPF 30
| Product NDC: | 0023-1134 |
| Proprietary Name: | M.D. FORTE Aftercare Environmental Protection Sunscreen SPF 30 |
| Non Proprietary Name: | octinoxate, octisalate, zinc oxide |
| Active Ingredient(s): | 75; 40; 78 mg/g; mg/g; mg/g & nbsp; octinoxate, octisalate, zinc oxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of M.D. FORTE Aftercare Environmental Protection Sunscreen SPF 30
| Product NDC: | 0023-1134 |
| Labeler Name: | Allergan, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 19980324 |
Package Information of M.D. FORTE Aftercare Environmental Protection Sunscreen SPF 30
| Package NDC: | 0023-1134-25 |
| Package Description: | 1 TUBE in 1 CARTON (0023-1134-25) > 75 g in 1 TUBE |
NDC Information of M.D. FORTE Aftercare Environmental Protection Sunscreen SPF 30
| NDC Code | 0023-1134-25 |
| Proprietary Name | M.D. FORTE Aftercare Environmental Protection Sunscreen SPF 30 |
| Package Description | 1 TUBE in 1 CARTON (0023-1134-25) > 75 g in 1 TUBE |
| Product NDC | 0023-1134 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | octinoxate, octisalate, zinc oxide |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 19980324 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Allergan, Inc. |
| Substance Name | OCTINOXATE; OCTISALATE; ZINC OXIDE |
| Strength Number | 75; 40; 78 |
| Strength Unit | mg/g; mg/g; mg/g |
| Pharmaceutical Classes |
