What is NDC 48951-1397?

48951-1397 is the product NDC for Aurum Hypericum, Magnesium hydroxide 4 [hp_X]/mL + 8 more ingredients liquid, listed with the FDA by Uriel Pharmacy, Inc. It has 1 package NDC, shown above in 10- and 11-digit form.

What is the active ingredient?

Magnesium hydroxide, Royal jelly, Silicon dioxide, Phosphoric acid, Strychnos ignatii seed, Gold trichloride, St. John's wort, Avena sativa flowering top, Oryctolagus cuniculus liver.

Uriel Pharmacy, Inc, NDC labeler code 48951. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Aurum Hypericum?

2 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Aurum Hypericum NDC 48951-1397 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)48951-1397Labeler and product segments. Claims need a package NDC.

Product NDC at billing width48951-1397Add 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
48951-1397-1	4895113970148951139701	10 AMPULE in 1 BOX (48951-1397-1) / 10 mL in 1 AMPULEMarketed from Sep 1, 2009

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): Aurum Hypericum
Generic name (nonproprietary): aurum hypericum
Active ingredients: Magnesium hydroxide — 4 [hp_X]/mLRoyal jelly — 6 [hp_X]/mLSilicon dioxide — 7 [hp_X]/mLPhosphoric acid — 5 [hp_X]/mLStrychnos ignatii seed — 5 [hp_X]/mLGold trichloride — 7 [hp_X]/mLSt. John's wort — 3 [hp_X]/mLAvena sativa flowering top — 3 [hp_X]/mLOryctolagus cuniculus liver — 4 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Uriel Pharmacy, IncNDC labeler code 48951
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Sep 1, 2009
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 48951-1397_2df4f968-af1e-82f1-e063-6294a90a65beSPL ID 2df4f968-af1e-82f1-e063-6294a90a65beSPL set ID 2df4f968-af1d-82f1-e063-6294a90a65beUNII NBZ3QY004S, L497I37F0C, ETJ7Z6XBU4, E4GA8884NN, 1NM3M2487K, 15443PR153, UFH8805FKA, MA9CQJ3F7F, 7A99K6361Z
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. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N448951139701 followed by a unit qualifier and the quantity

Package 48951-1397-01. 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 Feb 12, 2025.

Indications (excerpt from the label)

Directions: FOR ORAL USE.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 48951-1397

What is NDC 48951-1397?: 48951-1397 is the product NDC for Aurum Hypericum, Magnesium hydroxide 4 [hp_X]/mL + 8 more ingredients liquid, listed with the FDA by Uriel Pharmacy, Inc. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Aurum Hypericum.
What is the active ingredient?: Magnesium hydroxide, Royal jelly, Silicon dioxide, Phosphoric acid, Strychnos ignatii seed, Gold trichloride, St. John's wort, Avena sativa flowering top, Oryctolagus cuniculus liver.
Who is the labeler?: Uriel Pharmacy, Inc, NDC labeler code 48951. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Aurum Hypericum?: 2 other product NDCs are listed under this name. See all Aurum Hypericum NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Aurum Hypericum NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Aurum Hypericum	Oat 3 [hp_X]/1 + 8 more ingredients	PelletOral	Uriel Pharmacy Inc	48951-1281	48951-1281-02
Aurum Hypericum	Magnesium hydroxide 4 [hp_X]/mL + 8 more ingredients	LiquidOral	Uriel Pharmacy Inc.	48951-1368	48951-1368-03