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BB ANTI-FATIGUE ABSOLUTE SPF 25
BB ANTI-FATIGUE ABSOLUTE SPF 25 - 65371-025-02 - (HOMOSALATE, OCTISALATE, and OXYBENZONE)
Drug Information of BB ANTI-FATIGUE ABSOLUTE SPF 25
| Product NDC: | 65371-025 |
| Proprietary Name: | BB ANTI-FATIGUE ABSOLUTE SPF 25 |
| Non Proprietary Name: | HOMOSALATE, OCTISALATE, and OXYBENZONE |
| Active Ingredient(s): | 90; 45; 30 mg/mL; mg/mL; mg/mL & nbsp; HOMOSALATE, OCTISALATE, and OXYBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of BB ANTI-FATIGUE ABSOLUTE SPF 25
| Product NDC: | 65371-025 |
| Labeler Name: | ORLANE S.A. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130401 |
Package Information of BB ANTI-FATIGUE ABSOLUTE SPF 25
| Package NDC: | 65371-025-02 |
| Package Description: | 1 TUBE in 1 CARTON (65371-025-02) > 30 mL in 1 TUBE |
NDC Information of BB ANTI-FATIGUE ABSOLUTE SPF 25
| NDC Code | 65371-025-02 |
| Proprietary Name | BB ANTI-FATIGUE ABSOLUTE SPF 25 |
| Package Description | 1 TUBE in 1 CARTON (65371-025-02) > 30 mL in 1 TUBE |
| Product NDC | 65371-025 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | HOMOSALATE, OCTISALATE, and OXYBENZONE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20130401 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | ORLANE S.A. |
| Substance Name | HOMOSALATE; OCTISALATE; OXYBENZONE |
| Strength Number | 90; 45; 30 |
| Strength Unit | mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |
