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Severe Oral Pain Reliever
Severe Oral Pain Reliever - 0363-0838-51 - (Benzocaine)
Drug Information of Severe Oral Pain Reliever
| Product NDC: | 0363-0838 |
| Proprietary Name: | Severe Oral Pain Reliever |
| Non Proprietary Name: | Benzocaine |
| Active Ingredient(s): | 20 g/100g & nbsp; Benzocaine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Severe Oral Pain Reliever
| Product NDC: | 0363-0838 |
| Labeler Name: | Walgreens |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333B |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120110 |
Package Information of Severe Oral Pain Reliever
| Package NDC: | 0363-0838-51 |
| Package Description: | 1 BOTTLE, WITH APPLICATOR in 1 BLISTER PACK (0363-0838-51) > 14.17 g in 1 BOTTLE, WITH APPLICATOR (0363-0838-58) |
NDC Information of Severe Oral Pain Reliever
| NDC Code | 0363-0838-51 |
| Proprietary Name | Severe Oral Pain Reliever |
| Package Description | 1 BOTTLE, WITH APPLICATOR in 1 BLISTER PACK (0363-0838-51) > 14.17 g in 1 BOTTLE, WITH APPLICATOR (0363-0838-58) |
| Product NDC | 0363-0838 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Benzocaine |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20120110 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Walgreens |
| Substance Name | BENZOCAINE |
| Strength Number | 20 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
