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BABY ANBESOL
BABY ANBESOL - 0573-0216-25 - (benzocaine)
Drug Information of BABY ANBESOL
| Product NDC: | 0573-0216 |
| Proprietary Name: | BABY ANBESOL |
| Non Proprietary Name: | benzocaine |
| Active Ingredient(s): | 75 mg/g & nbsp; benzocaine |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of BABY ANBESOL
| Product NDC: | 0573-0216 |
| Labeler Name: | Wyeth Consumer Healthcare |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part356 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20040401 |
Package Information of BABY ANBESOL
| Package NDC: | 0573-0216-25 |
| Package Description: | 1 TUBE in 1 BLISTER PACK (0573-0216-25) > 9 g in 1 TUBE |
NDC Information of BABY ANBESOL
| NDC Code | 0573-0216-25 |
| Proprietary Name | BABY ANBESOL |
| Package Description | 1 TUBE in 1 BLISTER PACK (0573-0216-25) > 9 g in 1 TUBE |
| Product NDC | 0573-0216 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | benzocaine |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20040401 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Wyeth Consumer Healthcare |
| Substance Name | BENZOCAINE |
| Strength Number | 75 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
