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Hand-E XL
Hand-E XL - 62257-606-17 - (ALCOHOL)
Drug Information of Hand-E XL
| Product NDC: | 62257-606 |
| Proprietary Name: | Hand-E XL |
| Non Proprietary Name: | ALCOHOL |
| Active Ingredient(s): | .7 mL/mL & nbsp; ALCOHOL |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Hand-E XL
| Product NDC: | 62257-606 |
| Labeler Name: | ABC Compounding Co., Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333E |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20050401 |
Package Information of Hand-E XL
| Package NDC: | 62257-606-17 |
| Package Description: | 532 mL in 1 BOTTLE, PLASTIC (62257-606-17) |
NDC Information of Hand-E XL
| NDC Code | 62257-606-17 |
| Proprietary Name | Hand-E XL |
| Package Description | 532 mL in 1 BOTTLE, PLASTIC (62257-606-17) |
| Product NDC | 62257-606 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ALCOHOL |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20050401 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | ABC Compounding Co., Inc. |
| Substance Name | ALCOHOL |
| Strength Number | .7 |
| Strength Unit | mL/mL |
| Pharmaceutical Classes |
