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Antioxidant Day SPF 15
Antioxidant Day SPF 15 - 61016-0002-2 - (OCTINOXATE, OCTISALATE, OXYBENZONE)
Drug Information of Antioxidant Day SPF 15
| Product NDC: | 61016-0002 |
| Proprietary Name: | Antioxidant Day SPF 15 |
| Non Proprietary Name: | OCTINOXATE, OCTISALATE, OXYBENZONE |
| Active Ingredient(s): | 7.5; 3; 3 mL/100mL; mL/100mL; mL/100mL & nbsp; OCTINOXATE, OCTISALATE, OXYBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Antioxidant Day SPF 15
| Product NDC: | 61016-0002 |
| Labeler Name: | Columbia Cosmetics Manufacturing, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120419 |
Package Information of Antioxidant Day SPF 15
| Package NDC: | 61016-0002-2 |
| Package Description: | 59 mL in 1 BOTTLE (61016-0002-2) |
NDC Information of Antioxidant Day SPF 15
| NDC Code | 61016-0002-2 |
| Proprietary Name | Antioxidant Day SPF 15 |
| Package Description | 59 mL in 1 BOTTLE (61016-0002-2) |
| Product NDC | 61016-0002 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, OCTISALATE, OXYBENZONE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20120419 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Columbia Cosmetics Manufacturing, Inc. |
| Substance Name | OCTINOXATE; OCTISALATE; OXYBENZONE |
| Strength Number | 7.5; 3; 3 |
| Strength Unit | mL/100mL; mL/100mL; mL/100mL |
| Pharmaceutical Classes |
