Product NDC: | 59734-274 |
Proprietary Name: | Borba Age Defying |
Non Proprietary Name: | AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE, OCTOCRYLENE, and OXYBENZONE |
Active Ingredient(s): | 30; 100; 50; 50; 27.9; 60 mg/mL; mg/mL; mg/mL; mg/mL; mg/mL; mg/mL & nbsp; AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE, OCTOCRYLENE, and OXYBENZONE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 59734-274 |
Labeler Name: | Borba, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20110107 |
Package NDC: | 59734-274-29 |
Package Description: | 1 TUBE in 1 CARTON (59734-274-29) > 50 mL in 1 TUBE |
NDC Code | 59734-274-29 |
Proprietary Name | Borba Age Defying |
Package Description | 1 TUBE in 1 CARTON (59734-274-29) > 50 mL in 1 TUBE |
Product NDC | 59734-274 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE, OCTOCRYLENE, and OXYBENZONE |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20110107 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Borba, Inc. |
Substance Name | AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
Strength Number | 30; 100; 50; 50; 27.9; 60 |
Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL; mg/mL; mg/mL |
Pharmaceutical Classes |