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NDC 49973-667 · i-Health, Inc.

Generic nameCandida Albicans, Wood Creosote, Sodium Chloride, and Sulfur

Dosage formTABLET

RouteORAL

Active ingredient(s)CANDIDA ALBICANS, WOOD CREOSOTE, SODIUM CHLORIDE, SULFUR

Strength30; 12; 12; 30 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1

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

49973-667-20 — 20 BLISTER PACK in 1 BOX (49973-667-20) / 1 TABLET in 1 BLISTER PACK

49973-667-60 — 60 BLISTER PACK in 1 BOX (49973-667-60) / 1 TABLET in 1 BLISTER PACK

49973-667-62 — 120 BLISTER PACK in 1 BOX (49973-667-62) / 4 TABLET in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

49230-209 — Dextrose Monohydrate, Sodium Chloride, Sodium Lactate, Calcium Chloride, Magnesium Chloride, 49230-212 — Dextrose Monohydrate, Sodium Chloride, Sodium Lactate, Calcium Chloride, Magnesium Chloride, 49230-300 — Sodium Chloride, 49281-912 — Sodium Chloride, 49643-105 — Candida albicans, 49825-137 — Sulfur, Resorcinol, 49825-200 — Sulfur, 49967-415 — Sulfur, 49967-648 — Sulfur, 49967-895 — Sulfur, 50090-6521 — Polyethylene Glycol 3350, Sodium Sulfate Anhydrous, Sodium Bicarbonate, Sodium Chloride, Potassium Chloride, 50090-8020 — Polyethylene Glycol 3350, Sodium Sulfate Anhydrous, Sodium Bicarbonate, Sodium Chloride, Potassium Chloride, 50181-0034 — Coccus Cacti, Lung (Suis), Ignatia Amara, Causticum, Natrum Muriaticum, 50181-0078 — Mycoplasma Pneumoniae, Proteus (Vulgaris), Candida Albicans, Colibacillinum Cum Natrum Muriaticum, Mycobacterium Paratuberculosis,…, 50181-0084 — Phytolacca Decandra, Hypophysis (SUIS), Scrophularia Nodosa, Hypothalamus (SUIS), Calcarea Carbonica, Cimicifuga Racemosa, Lilium Tigrinum,…, 50405-850 — Sodium Sulfacetamide and Sulfur, 50405-851 — Sodium Sulfacetamide and Sulfur, 50405-852 — Sodium Sulfacetamide and Sulfur, 50718-0011 — Sulphur 12X, 50718-0012 — Sulphur 12X, +1373 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