Product NDC: | 51483-002 |
Proprietary Name: | Burn-B Gone OTC |
Non Proprietary Name: | Allantoin |
Active Ingredient(s): | .75 g/75g & nbsp; Allantoin |
Administration Route(s): | TOPICAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51483-002 |
Labeler Name: | DeWitt Laboratories, Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part347 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100601 |
Package NDC: | 51483-002-20 |
Package Description: | 75 g in 1 TUBE (51483-002-20) |
NDC Code | 51483-002-20 |
Proprietary Name | Burn-B Gone OTC |
Package Description | 75 g in 1 TUBE (51483-002-20) |
Product NDC | 51483-002 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Allantoin |
Dosage Form Name | GEL |
Route Name | TOPICAL |
Start Marketing Date | 20100601 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | DeWitt Laboratories, Inc |
Substance Name | ALLANTOIN |
Strength Number | .75 |
Strength Unit | g/75g |
Pharmaceutical Classes |