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De La Cruz Tincture of Iodine

NDC 24286-1528 · DLC Laboratories, Inc.

Generic nameIodine and Sodium Iodide and Alcohol

Dosage formLIQUID

RouteTOPICAL

Active ingredient(s)IODINE, SODIUM IODIDE, ALCOHOL

Strength470; 20; 20.4 mg/mL; mg/mL; mg/mL

Marketing categoryOTC MONOGRAPH DRUG

Packages

24286-1528-7 — 30 mL in 1 BOTTLE (24286-1528-7)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

21749-905 — Alcohol, 21749-906 — alcohol, 21749-907 — alcohol, 21749-908 — alcohol, 21749-909 — Alcohol, 21749-992 — alcohol, 21749-994 — alcohol, 21749-996 — alcohol, 21749-997 — alcohol, 23590-400 — Alcohol, 24286-1529 — Ethyl Alcohol, 24385-034 — Ethyl Alcohol, 24385-213 — Iodine and Sodium Iodide and Alcohol, 30142-088 — Iodine tincture, 30142-596 — Ethyl alcohol, 30142-849 — Alcohol, 30805-001 — Alcohol, 30805-003 — Alcohol, 30805-009 — Alcohol, 30805-012 — ALCOHOL, +2810 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