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Bio Iodine

NDC 43857-0088 · BioActive Nutritional, Inc.

Generic nameIodium

Dosage formLIQUID

RouteORAL

Active ingredient(s)IODINE

Strength6 [hp_X]/mL

Marketing categoryUNAPPROVED HOMEOPATHIC

Packages

43857-0088-1 — 30 mL in 1 BOTTLE, DROPPER (43857-0088-1)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

37662-1714 — Iodium, 37662-1715 — Iodium, 37662-1716 — Iodium, 37662-1717 — Iodium, 37662-1718 — Iodium, 37662-1719 — Iodium, 37662-1720 — Iodium, 37662-1721 — Iodium, 37662-1722 — Iodium, 41163-088 — Iodine, 48433-230 — Strong Iodine Solution, 49348-133 — IODINE, SODIUM IODIDE, ALCOHOL, 53645-2121 — Iodium, 53943-213 — Iodine and Sodium Iodide and Alcohol, 59450-030 — Iodine and Sodium Iodine and Alcohol, 62011-0117 — Iodine and Sodium Iodide and Alcohol, 63083-9205 — Anacardium Combination, 63868-330 — Iodine and Sodium Iodide and Alcohol, 66343-105 — Agaricus muscarius, Bufo rana, Cuprum met, Thyroidinum, Iodium, 69256-213 — Iodine and Sodium Iodide and Alcohol, +31 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