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NEUTRACETT
NEUTRACETT - 51435-001-01 - (ALLANTOIN GLYCERIN)
Drug Information of NEUTRACETT
| Product NDC: | 51435-001 |
| Proprietary Name: | NEUTRACETT |
| Non Proprietary Name: | ALLANTOIN GLYCERIN |
| Active Ingredient(s): | .5; 50 mg/.1g; mg/g & nbsp; ALLANTOIN GLYCERIN |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of NEUTRACETT
| Product NDC: | 51435-001 |
| Labeler Name: | ADVANCED BIOMEDICS INC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part347 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100528 |
Package Information of NEUTRACETT
| Package NDC: | 51435-001-01 |
| Package Description: | 28.3 g in 1 TUBE (51435-001-01) |
NDC Information of NEUTRACETT
| NDC Code | 51435-001-01 |
| Proprietary Name | NEUTRACETT |
| Package Description | 28.3 g in 1 TUBE (51435-001-01) |
| Product NDC | 51435-001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ALLANTOIN GLYCERIN |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20100528 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | ADVANCED BIOMEDICS INC |
| Substance Name | ALLANTOIN; GLYCERIN |
| Strength Number | .5; 50 |
| Strength Unit | mg/.1g; mg/g |
| Pharmaceutical Classes |
