RET Heart 7009 (ret heart) NDC 63083-7009

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-7009Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-7009Add 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
63083-7009-1	63083700901	29.5 mL in 1 BOTTLE, DROPPER (63083-7009-1)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): RET Heart 7009Suffix: 7009
Generic name (nonproprietary): ret heart
Active ingredients: Fagus sylvatica flowering top — 3 [hp_X]/29.5mLImpatiens glandulifera flower — 3 [hp_X]/29.5mLVerbena officinalis flowering top — 3 [hp_X]/29.5mLPotassium phosphate, Unspecified form — 3 [hp_X]/29.5mLMagnesium phosphate, Dibasic trihydrate — 3 [hp_X]/29.5mLSilicon dioxide — 3 [hp_X]/29.5mLAconitum napellus whole — 30 [hp_X]/29.5mLGold — 30 [hp_X]/29.5mLCausticum — 30 [hp_X]/29.5mLCoffea arabica seed, Roasted — 30 [hp_X]/29.5mLSaffron — 30 [hp_X]/29.5mLPulsatilla montana whole — 30 [hp_X]/29.5mL
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 Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Small Intestine Fluid/Electrolyte Absorption (Physiologic effect)Magnesium Ion Exchange Activity (Mechanism)Osmotic Activity (Mechanism)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)
Identifiers: Product ID 63083-7009_b042b517-d09c-41b3-a804-1d9993c53c11SPL ID b042b517-d09c-41b3-a804-1d9993c53c11SPL set ID e2bf8331-1c50-4216-93a4-1d3cf6404759UNII 21AF0IHY5U, AJU5O1A5ZV, 311PNK9CDZ, B7862WZ632, HF539G9L3Q, ETJ7Z6XBU4, U0NQ8555JD, 79Y1949PYO, DD5FO1WKFU, 9H58JRT35E, E849G4X5YJ, 24K790T39B
Pharmacologic class: Calculi Dissolution Agent; Osmotic Laxative; Standardized Chemical Allergen

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

N463083700901 followed by a unit qualifier and the quantity

Package 63083-7009-01. 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 Temporarily relieves indifference, intolerance, impatience, irritation, overenthusiasm, hyperactivity, dread, sadness, or anxiousness.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)