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Han-I-Foam
Han-I-Foam - 63533-855-55 - (ALCOHOL)
Drug Information of Han-I-Foam
| Product NDC: | 63533-855 |
| Proprietary Name: | Han-I-Foam |
| Non Proprietary Name: | ALCOHOL |
| Active Ingredient(s): | .62 mL/mL & nbsp; ALCOHOL |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Han-I-Foam
| Product NDC: | 63533-855 |
| Labeler Name: | Momar Incorporated |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333E |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20090901 |
Package Information of Han-I-Foam
| Package NDC: | 63533-855-55 |
| Package Description: | 208200 mL in 1 DRUM (63533-855-55) |
NDC Information of Han-I-Foam
| NDC Code | 63533-855-55 |
| Proprietary Name | Han-I-Foam |
| Package Description | 208200 mL in 1 DRUM (63533-855-55) |
| Product NDC | 63533-855 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ALCOHOL |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20090901 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Momar Incorporated |
| Substance Name | ALCOHOL |
| Strength Number | .62 |
| Strength Unit | mL/mL |
| Pharmaceutical Classes |
