| NDC Code | 13630-0217-4 |
|---|
| Package Description | 185 mL in 1 CAN (13630-0217-4) |
|---|
| Product NDC | 13630-0217 |
|---|
| Product Type Name | HUMAN OTC DRUG |
|---|
| Proprietary Name | Suntone |
|---|
| Proprietary Name Suffix | Sunscreen Broad Spectrum Spf30 |
|---|
| Non-Proprietary Name | Avobenzone, Homosalate, Octisalate, Octocrylene |
|---|
| Dosage Form | SPRAY |
|---|
| Usage | TOPICAL |
|---|
| Start Marketing Date | 20180430 |
|---|
| Marketing Category Name | OTC MONOGRAPH FINAL |
|---|
| Application Number | part352 |
|---|
| Manufacturer | Prime Packaging, Inc. |
|---|
| Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE |
|---|
| Strength | 25.2; 63; 42; 42 |
|---|
| Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL |
|---|