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PSORIASIS
PSORIASIS - 60512-6010-0 - (SULPHUR, ARSENICUM ALBUM, ALUMEN, MAGNESIA SULPHURICUM, NATRUM SULPHURICUM)
Drug Information of PSORIASIS
| Product NDC: | 60512-6010 |
| Proprietary Name: | PSORIASIS |
| Non Proprietary Name: | SULPHUR, ARSENICUM ALBUM, ALUMEN, MAGNESIA SULPHURICUM, NATRUM SULPHURICUM |
| Active Ingredient(s): | 8; 8; 8; 8; 8 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 & nbsp; SULPHUR, ARSENICUM ALBUM, ALUMEN, MAGNESIA SULPHURICUM, NATRUM SULPHURICUM |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, CHEWABLE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PSORIASIS
| Product NDC: | 60512-6010 |
| Labeler Name: | HOMEOLAB USA INC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20120711 |
Package Information of PSORIASIS
| Package NDC: | 60512-6010-0 |
| Package Description: | 90 TABLET, CHEWABLE in 1 BOTTLE (60512-6010-0) |
NDC Information of PSORIASIS
| NDC Code | 60512-6010-0 |
| Proprietary Name | PSORIASIS |
| Package Description | 90 TABLET, CHEWABLE in 1 BOTTLE (60512-6010-0) |
| Product NDC | 60512-6010 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | SULPHUR, ARSENICUM ALBUM, ALUMEN, MAGNESIA SULPHURICUM, NATRUM SULPHURICUM |
| Dosage Form Name | TABLET, CHEWABLE |
| Route Name | ORAL |
| Start Marketing Date | 20120711 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | HOMEOLAB USA INC |
| Substance Name | ARSENIC TRIOXIDE; MAGNESIUM SULFATE HEPTAHYDRATE; POTASSIUM ALUM; SODIUM SULFATE; SULFUR |
| Strength Number | 8; 8; 8; 8; 8 |
| Strength Unit | [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 |
| Pharmaceutical Classes |
