Home
>
National Drug Code (NDC)
>
Soothing Day SPF 15
Soothing Day SPF 15 - 63550-192-07 - (AVOBENZONE OCTINOXATE OXYBENZONE)
Drug Information of Soothing Day SPF 15
| Product NDC: | 63550-192 |
| Proprietary Name: | Soothing Day SPF 15 |
| Non Proprietary Name: | AVOBENZONE OCTINOXATE OXYBENZONE |
| Active Ingredient(s): | 20; 70; 50 mg/mL; mg/mL; mg/mL & nbsp; AVOBENZONE OCTINOXATE OXYBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Soothing Day SPF 15
| Product NDC: | 63550-192 |
| Labeler Name: | Kamins Dermatologics Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20101019 |
Package Information of Soothing Day SPF 15
| Package NDC: | 63550-192-07 |
| Package Description: | 50 mL in 1 BOX (63550-192-07) |
NDC Information of Soothing Day SPF 15
| NDC Code | 63550-192-07 |
| Proprietary Name | Soothing Day SPF 15 |
| Package Description | 50 mL in 1 BOX (63550-192-07) |
| Product NDC | 63550-192 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | AVOBENZONE OCTINOXATE OXYBENZONE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20101019 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Kamins Dermatologics Inc. |
| Substance Name | AVOBENZONE; OCTINOXATE; OXYBENZONE |
| Strength Number | 20; 70; 50 |
| Strength Unit | mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |
