What is NDC 58264-0164?

58264-0164 is the product NDC for D-153, Oyster shell calcium carbonate, Crude 30 [hp_X]/mL + 5 more ingredients solution, listed with the FDA by DNA Labs. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

D-153 (Juglans regia leaf, Lachesis, Calcarea carbonica, Lycopodium, Phosphorus, Magnesium Phosphate).

What is the active ingredient?

Oyster shell calcium carbonate, Crude, Juglans regia leaf, Lachesis muta venom, Lycopodium clavatum spore, Phosphorus, Magnesium phosphate, Dibasic trihydrate.

DNA Labs, NDC labeler code 58264. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for D-153?

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.

D-153 NDC 58264-0164 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)58264-0164Labeler and product segments. Claims need a package NDC.

Product NDC at billing width58264-0164Add 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
58264-0164-1	5826401640158264016401	29.57 mL in 1 BOTTLE, GLASS (58264-0164-1)Marketed from Feb 11, 2023

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): D-153
Generic name (nonproprietary): juglans regia leaf, lachesis, calcarea carbonica, lycopodium, phosphorus, magnesium phosphate
Active ingredients: Oyster shell calcium carbonate, Crude — 30 [hp_X]/mLJuglans regia leaf — 1 [hp_X]/mLLachesis muta venom — 30 [hp_X]/mLLycopodium clavatum spore — 30 [hp_X]/mLPhosphorus — 12 [hp_X]/mLMagnesium phosphate, Dibasic trihydrate — 6 [hp_X]/mL
Dosage form: Solution
Route: Sublingual
Labeler: DNA LabsNDC labeler code 58264
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Feb 11, 2023
Listing expires: Dec 31, 2026
Other FDA classes: 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 58264-0164_2b9f0ea7-160f-1707-e063-6394a90a3c44SPL ID 2b9f0ea7-160f-1707-e063-6394a90a3c44SPL set ID f473b88f-527c-46be-e053-2995a90a7300UNII 2E32821G6I, 85HKB87105, VSW71SS07I, C88X29Y479, 27YLU75U4W, HF539G9L3Q
Pharmacologic class: Calculi Dissolution Agent; Osmotic Laxative

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. Sublingual products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N458264016401 followed by a unit qualifier and the quantity

Package 58264-0164-01. 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 13, 2025.

Indications (excerpt from the label)

Temporary relief from symptoms associated with pancreas, liver or gall bladder weakness, inefficient insulin production and utilization.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 58264-0164

What is NDC 58264-0164?: 58264-0164 is the product NDC for D-153, Oyster shell calcium carbonate, Crude 30 [hp_X]/mL + 5 more ingredients solution, listed with the FDA by DNA Labs. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: D-153 (Juglans regia leaf, Lachesis, Calcarea carbonica, Lycopodium, Phosphorus, Magnesium Phosphate).
What is the active ingredient?: Oyster shell calcium carbonate, Crude, Juglans regia leaf, Lachesis muta venom, Lycopodium clavatum spore, Phosphorus, Magnesium phosphate, Dibasic trihydrate.
Who is the labeler?: DNA Labs, NDC labeler code 58264. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for D-153?: 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.