| Product NDC: | 76446-003 |
| Proprietary Name: | ANNA LOTAN Clear Protector Free Broad Spectrum SPF 32 Sunscreen |
| Non Proprietary Name: | HOMOSALATE, OCTISALATE, OXYBENZONE, AVOBENZONE, OCTOCRYLENE |
| Active Ingredient(s): | 3; 7.5; 5; 2.75; 4 mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp; HOMOSALATE, OCTISALATE, OXYBENZONE, AVOBENZONE, OCTOCRYLENE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 76446-003 |
| Labeler Name: | Anna Lotan Ltd |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120616 |
| Package NDC: | 76446-003-50 |
| Package Description: | 50 mL in 1 BOTTLE (76446-003-50) |
| NDC Code | 76446-003-50 |
| Proprietary Name | ANNA LOTAN Clear Protector Free Broad Spectrum SPF 32 Sunscreen |
| Package Description | 50 mL in 1 BOTTLE (76446-003-50) |
| Product NDC | 76446-003 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | HOMOSALATE, OCTISALATE, OXYBENZONE, AVOBENZONE, OCTOCRYLENE |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20120616 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Anna Lotan Ltd |
| Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
| Strength Number | 3; 7.5; 5; 2.75; 4 |
| Strength Unit | mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL |
| Pharmaceutical Classes |