| NDC Code | 59886-351-66 |
|---|
| Package Description | 200 g in 1 CAN (59886-351-66) |
|---|
| Product NDC | 59886-351 |
|---|
| Product Type Name | HUMAN OTC DRUG |
|---|
| Proprietary Name | Ultrasol |
|---|
| Proprietary Name Suffix | Sunscreen |
|---|
| Non-Proprietary Name | Avobenzone, Homosalate, Octinoxate, Octisalate, Octocrylene, Oxybenzone |
|---|
| Dosage Form | AEROSOL, SPRAY |
|---|
| Usage | TOPICAL |
|---|
| Start Marketing Date | 20100610 |
|---|
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
|---|
| Application Number | part352 |
|---|
| Manufacturer | Fischer Pharmaceuticals Ltd |
|---|
| Substance Name | AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
|---|
| Strength | 2.5; 5; 7.5; 5; 9; 5 |
|---|
| Strength Unit | g/100g; g/100g; g/100g; g/100g; g/100g; g/100g |
|---|