Product NDC: | 45156-5616 |
Proprietary Name: | Inflammation OTC |
Non Proprietary Name: | Allantoin |
Active Ingredient(s): | 3 g/600g & nbsp; Allantoin |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 45156-5616 |
Labeler Name: | Skin Deep |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part347 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100613 |
Package NDC: | 45156-5616-2 |
Package Description: | 1 TUBE in 1 BOX (45156-5616-2) > 29 g in 1 TUBE (45156-5616-1) |
NDC Code | 45156-5616-2 |
Proprietary Name | Inflammation OTC |
Package Description | 1 TUBE in 1 BOX (45156-5616-2) > 29 g in 1 TUBE (45156-5616-1) |
Product NDC | 45156-5616 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Allantoin |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20100613 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Skin Deep |
Substance Name | ALLANTOIN |
Strength Number | 3 |
Strength Unit | g/600g |
Pharmaceutical Classes |