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USFDA APPLICATION NUMBER - 50168 / DOSAGE - OINTMENT;TOPICAL - 400 UNITS/GM;1%;EQ 3.5MG BASE/GM;5,000 UNITS/GM **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
| Active Ingredient/Active Moiety | ||
| Ingredient Name | Basis of Strength | Strength |
|---|---|---|
| BACITRACIN ZINC(UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) | BACITRACIN | 400[iU] in 1 |
| HYDROCORTISONE(UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ) | HYDROCORTISONE | 10mg in 1 |
| NEOMYCIN SULFATE(UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) | NEOMYCIN | 3.5mg in 1 |
| POLYMYXIN B SULFATE(UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K) | POLYMYXIN B | 5000[iU] in 1 |
Inactive Ingredients
| Ingredient Name | Pfizer Laboratories Div Pfizer Inc |
|---|---|
| PETROLATUM(4T6H12BN9U) |
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