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SUNBAR SPF 15
SUNBAR SPF 15 - 63550-810-12 - (AVOBENZONE HOMOSALATE OCTISALATE OXYBENZONE)
Drug Information of SUNBAR SPF 15
| Product NDC: | 63550-810 |
| Proprietary Name: | SUNBAR SPF 15 |
| Non Proprietary Name: | AVOBENZONE HOMOSALATE OCTISALATE OXYBENZONE |
| Active Ingredient(s): | 30; 100; 50; 60 mg/mL; mg/mL; mg/mL; mg/mL & nbsp; AVOBENZONE HOMOSALATE OCTISALATE OXYBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SPRAY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SUNBAR SPF 15
| Product NDC: | 63550-810 |
| Labeler Name: | Kamins Dermatologics Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100930 |
Package Information of SUNBAR SPF 15
| Package NDC: | 63550-810-12 |
| Package Description: | 150 mL in 1 BOX (63550-810-12) |
NDC Information of SUNBAR SPF 15
| NDC Code | 63550-810-12 |
| Proprietary Name | SUNBAR SPF 15 |
| Package Description | 150 mL in 1 BOX (63550-810-12) |
| Product NDC | 63550-810 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | AVOBENZONE HOMOSALATE OCTISALATE OXYBENZONE |
| Dosage Form Name | SPRAY |
| Route Name | TOPICAL |
| Start Marketing Date | 20100930 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Kamins Dermatologics Inc. |
| Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OXYBENZONE |
| Strength Number | 30; 100; 50; 60 |
| Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |
