What is NDC 63083-7005?

63083-7005 is the product NDC for RET Kidney 7005 (ret kidney), Populus tremula flowering top 3 [hp_X]/29.5mL + 12 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 is the active ingredient?

Populus tremula flowering top, Mimulus guttatus flowering top, Pinus sylvestris flowering top, Calcium sulfate anhydrous, Potassium phosphate, Unspecified form, Silver nitrate, Gold, Oyster shell calcium carbonate, Crude, Graphite, Strychnos ignatii seed, Lycopodium clavatum spore, Phosphorus, Sepia officinalis juice.

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 Kidney 7005?

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 Kidney 7005 NDC 63083-7005 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-7005Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-7005Add 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
63083-7005-1	6308370050163083700501	29.5 mL in 1 BOTTLE, DROPPER (63083-7005-1)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 Kidney 7005Suffix: 7005
Generic name (nonproprietary): ret kidney
Active ingredients: Populus tremula flowering top — 3 [hp_X]/29.5mLMimulus guttatus flowering top — 3 [hp_X]/29.5mLPinus sylvestris flowering top — 3 [hp_X]/29.5mLCalcium sulfate anhydrous — 3 [hp_X]/29.5mLPotassium phosphate, Unspecified form — 3 [hp_X]/29.5mLSilver nitrate — 30 [hp_X]/29.5mLGold — 30 [hp_X]/29.5mLOyster shell calcium carbonate, Crude — 30 [hp_X]/29.5mLGraphite — 30 [hp_X]/29.5mLStrychnos ignatii seed — 30 [hp_X]/29.5mLLycopodium clavatum spore — 30 [hp_X]/29.5mLPhosphorus — 30 [hp_X]/29.5mLSepia officinalis juice — 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: Allergens (Chemical structure)Calcium (Chemical structure)Divalent (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Coagulation Factor Activity (Physiologic effect)Increased Histamine Release (Physiologic effect)Phosphate Chelating Activity (Mechanism)
Identifiers: Product ID 63083-7005_ce57b1da-4d72-4c34-b5d4-ed9c7d3d4c7cSPL ID ce57b1da-4d72-4c34-b5d4-ed9c7d3d4c7cSPL set ID 017f4c37-3eec-4078-9ce6-aca52fd4974dUNII 5Q01F7TPJJ, 192426I5JU, 2HEM73YI9I, E934B3V59H, B7862WZ632, 95IT3W8JZE, 79Y1949PYO, 2E32821G6I, 4QQN74LH4O, 1NM3M2487K, C88X29Y479, 27YLU75U4W, QDL83WN8C2
Pharmacologic class: Blood Coagulation Factor; Phosphate Binder; 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

N463083700501 followed by a unit qualifier and the quantity

Package 63083-7005-01. 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 fear, worry, dread, lack of courage, shame, self-reproach, anxiousness, unworthiness, or irritability.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 63083-7005

What is NDC 63083-7005?: 63083-7005 is the product NDC for RET Kidney 7005 (ret kidney), Populus tremula flowering top 3 [hp_X]/29.5mL + 12 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 Kidney 7005 (RET Kidney).
What is the active ingredient?: Populus tremula flowering top, Mimulus guttatus flowering top, Pinus sylvestris flowering top, Calcium sulfate anhydrous, Potassium phosphate, Unspecified form, Silver nitrate, Gold, Oyster shell calcium carbonate, Crude, Graphite, Strychnos ignatii seed, Lycopodium clavatum spore, Phosphorus, Sepia officinalis juice.
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 Kidney 7005?: 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 Kidney 7005 (Ret kidney) NDC 63083-7005