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IONTOPHORESIS
IONTOPHORESIS - 51985-010-01 - (ALLANTOIN)
Drug Information of IONTOPHORESIS
| Product NDC: | 51985-010 |
| Proprietary Name: | IONTOPHORESIS |
| Non Proprietary Name: | ALLANTOIN |
| Active Ingredient(s): | .1 mL/20mL & nbsp; ALLANTOIN |
| Administration Route(s): | CUTANEOUS |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of IONTOPHORESIS
| Product NDC: | 51985-010 |
| Labeler Name: | ROCKET ELECTRIC CO., LTD. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part347 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100401 |
Package Information of IONTOPHORESIS
| Package NDC: | 51985-010-01 |
| Package Description: | 20 mL in 1 CARTON (51985-010-01) |
NDC Information of IONTOPHORESIS
| NDC Code | 51985-010-01 |
| Proprietary Name | IONTOPHORESIS |
| Package Description | 20 mL in 1 CARTON (51985-010-01) |
| Product NDC | 51985-010 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ALLANTOIN |
| Dosage Form Name | LOTION |
| Route Name | CUTANEOUS |
| Start Marketing Date | 20100401 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | ROCKET ELECTRIC CO., LTD. |
| Substance Name | ALLANTOIN |
| Strength Number | .1 |
| Strength Unit | mL/20mL |
| Pharmaceutical Classes |
