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SUNBAR SPF 30
SUNBAR SPF 30 - 63550-811-10 - (Avobenzone Octinoxate Oxybenzone Titanium dioxide)
Drug Information of SUNBAR SPF 30
| Product NDC: | 63550-811 |
| Proprietary Name: | SUNBAR SPF 30 |
| Non Proprietary Name: | Avobenzone Octinoxate Oxybenzone Titanium dioxide |
| Active Ingredient(s): | 25; 75; 6; 20 mg/mL; mg/mL; mg/mL; mg/mL & nbsp; Avobenzone Octinoxate Oxybenzone Titanium dioxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SUNBAR SPF 30
| Product NDC: | 63550-811 |
| Labeler Name: | Kamins Dermatologics Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20101015 |
Package Information of SUNBAR SPF 30
| Package NDC: | 63550-811-10 |
| Package Description: | 120 mL in 1 BOX (63550-811-10) |
NDC Information of SUNBAR SPF 30
| NDC Code | 63550-811-10 |
| Proprietary Name | SUNBAR SPF 30 |
| Package Description | 120 mL in 1 BOX (63550-811-10) |
| Product NDC | 63550-811 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Avobenzone Octinoxate Oxybenzone Titanium dioxide |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20101015 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Kamins Dermatologics Inc. |
| Substance Name | AVOBENZONE; OCTINOXATE; OXYBENZONE; TITANIUM DIOXIDE |
| Strength Number | 25; 75; 6; 20 |
| Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |
