Product NDC: | 49715-013 |
Proprietary Name: | Homme Aqua Sun Block SPF50 Plus PA 2Plus |
Non Proprietary Name: | OCTINOXATE, OCTISALATE, ENSULIZOLE, BEMOTRIZINOL, AVOBENZONE |
Active Ingredient(s): | 1.305; 1.305; 1.74; 3.26; 2.175 g/43.5g; g/43.5g; g/43.5g; g/43.5g; g/43.5g & nbsp; OCTINOXATE, OCTISALATE, ENSULIZOLE, BEMOTRIZINOL, AVOBENZONE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49715-013 |
Labeler Name: | WIZCOZ CORPORATION LTD |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20111201 |
Package NDC: | 49715-013-43 |
Package Description: | 43.5 g in 1 BOTTLE, PLASTIC (49715-013-43) |
NDC Code | 49715-013-43 |
Proprietary Name | Homme Aqua Sun Block SPF50 Plus PA 2Plus |
Package Description | 43.5 g in 1 BOTTLE, PLASTIC (49715-013-43) |
Product NDC | 49715-013 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTINOXATE, OCTISALATE, ENSULIZOLE, BEMOTRIZINOL, AVOBENZONE |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20111201 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | WIZCOZ CORPORATION LTD |
Substance Name | AVOBENZONE; BEMOTRIZINOL; ENSULIZOLE; OCTINOXATE; OCTISALATE |
Strength Number | 1.305; 1.305; 1.74; 3.26; 2.175 |
Strength Unit | g/43.5g; g/43.5g; g/43.5g; g/43.5g; g/43.5g |
Pharmaceutical Classes |