Product NDC: | 61047-824 |
Proprietary Name: | Purpose |
Non Proprietary Name: | Octinoxate, Octisalate, and Oxybenzone |
Active Ingredient(s): | 9; 6; 3.6 g/120g; g/120g; g/120g & nbsp; Octinoxate, Octisalate, and Oxybenzone |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 61047-824 |
Labeler Name: | KIK Custom Products |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20130408 |
Package NDC: | 61047-824-94 |
Package Description: | 120 g in 1 BOTTLE (61047-824-94) |
NDC Code | 61047-824-94 |
Proprietary Name | Purpose |
Package Description | 120 g in 1 BOTTLE (61047-824-94) |
Product NDC | 61047-824 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Octinoxate, Octisalate, and Oxybenzone |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20130408 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | KIK Custom Products |
Substance Name | OCTINOXATE; OCTISALATE; OXYBENZONE |
Strength Number | 9; 6; 3.6 |
Strength Unit | g/120g; g/120g; g/120g |
Pharmaceutical Classes |