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Candida
Candida - 43742-0091-1 - (Candida Albicans)
Drug Information of Candida
| Product NDC: | 43742-0091 |
| Proprietary Name: | Candida |
| Non Proprietary Name: | Candida Albicans |
| Active Ingredient(s): | 200 [hp_C]/mL & nbsp; Candida Albicans |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Candida
| Product NDC: | 43742-0091 |
| Labeler Name: | DeseretBiolgicals, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20120822 |
Package Information of Candida
| Package NDC: | 43742-0091-1 |
| Package Description: | 30 mL in 1 BOTTLE, DROPPER (43742-0091-1) |
NDC Information of Candida
| NDC Code | 43742-0091-1 |
| Proprietary Name | Candida |
| Package Description | 30 mL in 1 BOTTLE, DROPPER (43742-0091-1) |
| Product NDC | 43742-0091 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Candida Albicans |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20120822 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | DeseretBiolgicals, Inc |
| Substance Name | CANDIDA ALBICANS |
| Strength Number | 200 |
| Strength Unit | [hp_C]/mL |
| Pharmaceutical Classes |
