Hypotonia Drops 2030 (hypotonia drops) NDC 63083-2030

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-2030Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-2030Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
63083-2030-2	63083203002	59 mL in 1 BOTTLE, DROPPER (63083-2030-2)Marketed from Aug 15, 1985

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Hypotonia Drops 2030Suffix: 2030
Generic name (nonproprietary): hypotonia drops
Active ingredients: Hawthorn leaf with flower — 1 [hp_X]/59mLAsian ginseng — 2 [hp_X]/59mLCytisus scoparius flowering top — 3 [hp_X]/59mLPrunus laurocerasus leaf — 3 [hp_X]/59mLNerium oleander whole — 4 [hp_X]/59mLSus scrofa adrenal gland — 6 [hp_X]/59mLBeef kidney — 6 [hp_X]/59mLAngiotensin i — 12 [hp_X]/59mL
Dosage form: Liquid
Route: Oral
Labeler: Professional Complementary Health Formulas
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Aug 15, 1984
Listing expires: Dec 31, 2027
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)
Identifiers: Product ID 63083-2030_3fcb60a5-b9b1-4f9e-933d-c1fc6c4128a7SPL ID 3fcb60a5-b9b1-4f9e-933d-c1fc6c4128a7SPL set ID e6f00aaa-e90b-4c06-b5be-120ffa14f771UNII 6OM09RPY36, CUQ3A77YXI, XZC6H8R666, F26P2D4757, JG9V5H8412, 398IYQ16YV, 5HOC10FSIC, 9C880YQG7C
Pharmacologic class: Non-Standardized Plant Allergenic Extract

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N463083203002 followed by a unit qualifier and the quantity

Package 63083-2030-02. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Jan 8, 2026.

Indications (excerpt from the label)

INDICATIONS For the temporary relief of dizziness, fatigue, nausea, weakened memory, or slow perception.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)