Home
>
National Drug Code (NDC)
>
DAY L
DAY L - 63550-122-03 - (AVOBENZONE OCTISALATE OCTINOXATE)
Drug Information of DAY L
| Product NDC: | 63550-122 |
| Proprietary Name: | DAY L |
| Non Proprietary Name: | AVOBENZONE OCTISALATE OCTINOXATE |
| Active Ingredient(s): | 25; 75; 40 mg/mL; mg/mL; mg/mL & nbsp; AVOBENZONE OCTISALATE OCTINOXATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DAY L
| Product NDC: | 63550-122 |
| Labeler Name: | Kamins Dermatologics Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120307 |
Package Information of DAY L
| Package NDC: | 63550-122-03 |
| Package Description: | 50 mL in 1 BOX (63550-122-03) |
NDC Information of DAY L
| NDC Code | 63550-122-03 |
| Proprietary Name | DAY L |
| Package Description | 50 mL in 1 BOX (63550-122-03) |
| Product NDC | 63550-122 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | AVOBENZONE OCTISALATE OCTINOXATE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20120307 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Kamins Dermatologics Inc. |
| Substance Name | AVOBENZONE; OCTINOXATE; OCTISALATE |
| Strength Number | 25; 75; 40 |
| Strength Unit | mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |
