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Hormone Harmony

NDC 70558-0008 · Pro Weight Loss Inc.

Generic nameAcetaldehyde, Dopamine Hydrochloride, DHEA (Dehydroepiandrosterone), 7-Oxo- Dehydroepiandrosterone 3-Acetate, Folliculinum, Oophorinum (Suis), Cholesterinum, Progesterone, Testosterone, Cortisone Aceticum, Aldosterone, Androsterone, Follicle Stimulating Hormone
Dosage formLIQUID
RouteORAL
Active ingredient(s)ACETALDEHYDE, DOPAMINE HYDROCHLORIDE, PRASTERONE, 7-KETO-DEHYDROEPIANDROSTERONE, ESTRONE, SUS SCROFA OVARY, CHOLESTEROL, PROGESTERONE, TESTOSTERONE, CORTISONE ACETATE, ALDOSTERONE, ANDROSTERONE, FOLLITROPIN
Strength8; 6; 12; 12; 8; 12; 6; 8; 12; 6; 8; 8; 8 [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Pharmacologic classAndrogen Receptor Agonists [MoA], Androgen [EPC], Androstanes [CS], Catecholamine [EPC], Catecholamines [CS], Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC], Gonadotropin [EPC], Gonadotropins [CS], Progesterone [CS], Progesterone [EPC]
DEA scheduleCIII
Marketing categoryUNAPPROVED HOMEOPATHIC

Packages

70558-0008-1 — 30 mL in 1 BOTTLE, DROPPER (70558-0008-1)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

69311-0005 — Asclepias Vincetoxicum, Echinacea (Angustifolia), Hypothalamus (Suis), Cerebrum (Suis), Hepar Suis, Kidney (Suis), Methylcobalamin,…, 69452-148 — PROGESTERONE, 69452-149 — PROGESTERONE, 69452-233 — PROGESTERONE, 69452-234 — PROGESTERONE, 70095-136 — Progesterone, 70518-2560 — Progesterone, 70518-4166 — PROGESTERONE, 70518-4552 — Progesterone, 70558-0007 — Adenosinum Triphosphoricum Dinatrum, Adrenal Cortex (Suis), Bacopa Speciosa, Equol, Pantothenic Acid, Rhodiola, Stomach (Suis), Chininum…, 70558-0009 — Sarcolacticum Acidum, Viscum Album, Iodium, Fucus Vesiculosus, Galium Aparine, Natrum Oxalaceticum, Thyroidinum (Suis), DHEA…, 70700-112 — Testosterone, 70700-162 — Progesterone, 70700-163 — Progesterone, 70700-201 — Progesterone, 70700-286 — PROGESTERONE, 71205-669 — Progesterone, 71205-684 — Progesterone, 71205-902 — Progesterone, 71205-903 — Progesterone, +418 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