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DAY C
DAY C - 63550-120-03 - (AVOBENZONE OCTINOXATE OXYBENZONE)
Drug Information of DAY C
| Product NDC: | 63550-120 |
| Proprietary Name: | DAY C |
| Non Proprietary Name: | AVOBENZONE OCTINOXATE OXYBENZONE |
| Active Ingredient(s): | 20; 70; 50 mg/g; mg/g; mg/g & nbsp; AVOBENZONE OCTINOXATE OXYBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DAY C
| Product NDC: | 63550-120 |
| Labeler Name: | Kamins Dermatologics Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120312 |
Package Information of DAY C
| Package NDC: | 63550-120-03 |
| Package Description: | 50 g in 1 BOX (63550-120-03) |
NDC Information of DAY C
| NDC Code | 63550-120-03 |
| Proprietary Name | DAY C |
| Package Description | 50 g in 1 BOX (63550-120-03) |
| Product NDC | 63550-120 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | AVOBENZONE OCTINOXATE OXYBENZONE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20120312 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Kamins Dermatologics Inc. |
| Substance Name | AVOBENZONE; OCTINOXATE; OXYBENZONE |
| Strength Number | 20; 70; 50 |
| Strength Unit | mg/g; mg/g; mg/g |
| Pharmaceutical Classes |
