Home
>
National Drug Code (NDC)
>
UltrasolSunscreen
UltrasolSunscreen - 59886-337-77 - (Avobenzone, Octinoxate, Octisalate, Oxybenzone)
Drug Information of UltrasolSunscreen
| Product NDC: | 59886-337 |
| Proprietary Name: | UltrasolSunscreen |
| Non Proprietary Name: | Avobenzone, Octinoxate, Octisalate, Oxybenzone |
| Active Ingredient(s): | 2; 7.5; 5; 4 g/100g; g/100g; g/100g; g/100g & nbsp; Avobenzone, Octinoxate, Octisalate, Oxybenzone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of UltrasolSunscreen
| Product NDC: | 59886-337 |
| Labeler Name: | Fischer Pharmaceuticals Ltd |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100301 |
Package Information of UltrasolSunscreen
| Package NDC: | 59886-337-77 |
| Package Description: | 1 TUBE in 1 BOX (59886-337-77) > 50 g in 1 TUBE |
NDC Information of UltrasolSunscreen
| NDC Code | 59886-337-77 |
| Proprietary Name | UltrasolSunscreen |
| Package Description | 1 TUBE in 1 BOX (59886-337-77) > 50 g in 1 TUBE |
| Product NDC | 59886-337 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Avobenzone, Octinoxate, Octisalate, Oxybenzone |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20100301 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Fischer Pharmaceuticals Ltd |
| Substance Name | AVOBENZONE; OCTINOXATE; OCTISALATE; OXYBENZONE |
| Strength Number | 2; 7.5; 5; 4 |
| Strength Unit | g/100g; g/100g; g/100g; g/100g |
| Pharmaceutical Classes |
