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 |