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CAND HOMO

NDC 43742-2190 · Deseret Biologicals, Inc.

Generic nameCandida Albicans, Candida Albicans DNA, Candida Parapsilosis, Candida Parapsilosis DNA
Dosage formLIQUID
RouteORAL
Active ingredient(s)CANDIDA ALBICANS, CANDIDA ALBICANS DNA, CANDIDA PARAPSILOSIS, CANDIDA PARAPSILOSIS DNA
Strength15; 15; 15; 15 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Pharmacologic classAllergens [CS], Cell-mediated Immunity [PE], Fungal Proteins [CS], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Fungal Allergenic Extract [EPC]
Marketing categoryUNAPPROVED HOMEOPATHIC

Packages

43742-2190-1 — 30 mL in 1 BOTTLE, DROPPER (43742-2190-1)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

22840-5610 — Candida albicans, 22840-9642 — Candida albicans and Neurospora intermedia, 22840-9643 — Candida albicans and Neurospora intermedia, 22840-9644 — Candida albicans and Neurospora intermedia, 22840-9645 — Candida albicans and Neurospora intermedia, 22840-9677 — Candida albicans and Neurospora intermedia, 43742-1741 — Candida Albicans, 43742-1743 — Candida Albicans, 43742-1745 — Candida Albicans, 43742-1760 — Alternaria Tenuis Nees, Aspergillus Niger, Torula Cerevisiae, Candida Albicans, Candida Parapsilosis, Mucor Racemosus, Rhizopus Nigricans,…, 43742-2237 — Alternaria Tenuis Nees, Aspergillus Niger, Candida Albicans, Candida Krusei, Candida Parapsilosis, Candida Tropicalis, Mucor Racemosus,…, 43742-2547 — Alternaria Alternata, Aspergillus Niger, Candida Albicans, Candida Krusei, Candida Parapsilosis, Candida Tropicalis, Mucor Racemosus,…, 43857-0177 — Candida Albicans, 43857-0184 — Candida Albicans, 43857-0185 — Candida Albicans, 43857-0247 — Candida Albicans, 43857-0251 — Candida Albicans, 43857-0303 — Candida Albicans, 43857-0415 — Candida Albicans, 43857-0525 — Arsenicum Album, Phosphorus, Pulsatilla (Pratensis), Sepia, Aspergillus Niger, Candida Albicans, Candida Parapsilosis, Torula Cerevisiae,…, +74 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels