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Transform 30

NDC 80814-0001 · H2 Nutrition

FDA lists marketing as ended on 2026-09-03.
Generic nameFucus Vesiculosus, Cysteinum, Nicotinamidum, Alpha-Lipoicum Acidum, Antimonium Crudum, Chromium Sulphuricum, Gambogia, Anacardium Orientale, Graphites
Dosage formLIQUID
RouteORAL
Active ingredient(s)FUCUS VESICULOSUS, CYSTEINE, NIACINAMIDE, ALPHA LIPOIC ACID, ANTIMONY TRISULFIDE, CHROMIC SULFATE PENTADECAHYDRATE, GAMBOGE, SEMECARPUS ANACARDIUM JUICE, GRAPHITE
Strength12; 12; 12; 6; 3; 12; 30; 6; 30 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL
Marketing categoryUNAPPROVED HOMEOPATHIC

Packages

80814-0001-1 — 60 mL in 1 BOTTLE, DROPPER (80814-0001-1)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

75826-169 — Sodium Fluoride, 75826-170 — Sodium Fluoride, 75826-171 — Sodium Fluoride, 75854-314 — .beta.-carotene, ascorbic acid, cholecalciferol, .alpha.-tocopherol acetate, dl-, thiamine mononitrate, riboflavin, niacinamide, pyridoxine…, 75854-343 — niacinamide, zinc glycinate, levomefolate calcium, cupric oxide, selenium and chromium, 77931-0001 — Fucus Vesiculosus, Chelidonium Majus, Kali Phosphoricum, Lycopodium Clavatum, Natrum Muriaticum, Quercus Glandium Spiritus, Quercus Robur,…, 77964-002 — niacinamide, adenosine, 77964-003 — niacinamide, adenosine, 77964-004 — niacinamide, adenosine, 77964-006 — niacinamide, adenosine, 81825-0006 — Arsenicum Album, Arsenicum Iodatum, Borax, Calcarea Carbonica, Graphites, Mezereum, Proteus, Natrum Muriaticum, Phytolacca Decandra, Sepia,…, 81825-0012 — artemisia vulgaris root, chelidonium majus whole, punica granatum root bark, spigelia anthelmia whole, krameria lappacea root, arsenic…, 82083-0001 — niacinamide, adenosine, 82083-0002 — niacinamide, adenosine, 82083-0003 — niacinamide, adenosine, 82083-0004 — niacinamide, adenosine, 82083-0005 — niacinamide, adenosine, 82083-0006 — niacinamide, adenosine, 82083-0010 — niacinamide, adenosine, 82083-0013 — adenosine, niacinamide, +739 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