What is NDC 63083-7007?

63083-7007 is the product NDC for RET Gallbladder 7007 (ret gallbladder), Ulex europaeus flower 3 [hp_X]/29.5mL + 8 more ingredients liquid, listed with the FDA by Professional Complementary Health Formulas. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

RET Gallbladder 7007 (RET Gallbladder).

What is the active ingredient?

Ulex europaeus flower, Eleutherococcus senticosus root oil, Salix alba flowering top, Potassium phosphate, Unspecified form, Copper, Lachesis muta venom, Lycopodium clavatum spore, Sodium chloride, Datura stramonium.

Professional Complementary Health Formulas, NDC labeler code 63083. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for RET Gallbladder 7007?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

RET Gallbladder 7007 NDC 63083-7007

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-7007Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-7007Add 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
63083-7007-1	6308370070163083700701	29.5 mL in 1 BOTTLE, DROPPER (63083-7007-1)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 Gallbladder 7007Suffix: 7007
Generic name (nonproprietary): ret gallbladder
Active ingredients: Ulex europaeus flower — 3 [hp_X]/29.5mLEleutherococcus senticosus root oil — 3 [hp_X]/29.5mLSalix alba flowering top — 3 [hp_X]/29.5mLPotassium phosphate, Unspecified form — 3 [hp_X]/29.5mLCopper — 30 [hp_X]/29.5mLLachesis muta venom — 30 [hp_X]/29.5mLLycopodium clavatum spore — 30 [hp_X]/29.5mLSodium chloride — 30 [hp_X]/29.5mLDatura stramonium — 30 [hp_X]/29.5mL
Dosage form: Liquid
Route: Oral
Labeler: Professional Complementary Health FormulasNDC labeler code 63083
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Aug 15, 1984
Listing expires: Dec 31, 2027
Other FDA classes: Copper (Chemical structure)Decreased Embryonic Implantation (Physiologic effect)Decreased Sperm Motility (Physiologic effect)Inhibit Ovum Fertilization (Physiologic effect)
Identifiers: Product ID 63083-7007_b82992bf-fb5e-4189-8bc5-531d8268b0b1SPL ID b82992bf-fb5e-4189-8bc5-531d8268b0b1SPL set ID 82bc7b50-aea3-4993-b171-919940fef297UNII 398DBS1PXN, 0DAF87OMMD, XBP5X7E70R, B7862WZ632, 789U1901C5, VSW71SS07I, C88X29Y479, 451W47IQ8X, G6W4F0V8Z3
Pharmacologic class: Copper-containing Intrauterine Device

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

N463083700701 followed by a unit qualifier and the quantity

Package 63083-7007-01. 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 resentment, bitterness, self-pity, hopelessness, pessimism, self-perfection, dread, or anxiousness.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 63083-7007

What is NDC 63083-7007?: 63083-7007 is the product NDC for RET Gallbladder 7007 (ret gallbladder), Ulex europaeus flower 3 [hp_X]/29.5mL + 8 more ingredients liquid, listed with the FDA by Professional Complementary Health Formulas. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: RET Gallbladder 7007 (RET Gallbladder).
What is the active ingredient?: Ulex europaeus flower, Eleutherococcus senticosus root oil, Salix alba flowering top, Potassium phosphate, Unspecified form, Copper, Lachesis muta venom, Lycopodium clavatum spore, Sodium chloride, Datura stramonium.
Who is the labeler?: Professional Complementary Health Formulas, NDC labeler code 63083. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for RET Gallbladder 7007?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

RET Gallbladder 7007 (Ret gallbladder) NDC 63083-7007