Home
>
National Drug Code (NDC)
>
Burn-B Gone OTC
Burn-B Gone OTC - 51483-002-20 - (Allantoin)
Drug Information of Burn-B Gone OTC
| 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) |
Labeler Information of Burn-B Gone OTC
| 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 Information of Burn-B Gone OTC
| Package NDC: | 51483-002-20 |
| Package Description: | 75 g in 1 TUBE (51483-002-20) |
NDC Information of Burn-B Gone OTC
| 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 |
