apo-STOM NDC 59469-102

NDC codes

FDA NDC Directory

Product NDC (as listed)59469-102Labeler and product segments. Claims need a package NDC.

Product NDC at billing width59469-0102Add 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
59469-102-10	59469010210	1 BOTTLE, GLASS in 1 BOX (59469-102-10) / 50 mL in 1 BOTTLE, GLASSMarketed from Dec 11, 2008

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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): apo-STOM
Generic name (nonproprietary): antimony trisulfide, atropa bella-donna flowering top, colchicum autumnale bulb, citrullus colocynthis fruit pulp, sodium phosphate, strychnos nux-vomica seed, robinia pseudoacacia bark, and achillea millefolium flowering top
Active ingredients: Antimony trisulfide — 8 [hp_X]/50mLAtropa bella-donna flowering top — 4 [hp_X]/50mLColchicum autumnale bulb — 6 [hp_X]/50mLCitrullus colocynthis fruit pulp — 4 [hp_X]/50mLSodium phosphate — 4 [hp_X]/50mLStrychnos nux-vomica seed — 4 [hp_X]/50mLRobinia pseudoacacia bark — 6 [hp_X]/50mLAchillea millefolium flowering top — 2606 mg/50mL
Dosage form: Solution/ drops
Route: Oral
Labeler: PEKANA Naturheilmittel GmbH
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Dec 11, 2008
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 59469-102_3634624b-0eb8-490f-b9b5-1a0ae69ab805SPL ID 3634624b-0eb8-490f-b9b5-1a0ae69ab805SPL set ID 5ded31e3-c7fb-473f-9f37-13ee9cad386cUNII F79059A38U, B26WXN5GZJ, 993QHL78E6, 23H32AOH17, SE337SVY37, 269XH13919, 7TPC058OWY, 55862Q3XEU
Pharmacologic class: Non-Standardized Plant Allergenic Extract

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

N459469010210 followed by a unit qualifier and the quantity

Package 59469-0102-10. 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 Dec 6, 2022.

Indications (excerpt from the label)

Indications For maintenance of normal stomach health. Application of this homeopathic remedy for the designated usage is exclusively based on homeopathic experience. With severe forms of this disease, a clinically proven therapy is indicated.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)