Ohm-Inma NDC 66096-757

NDC codes

FDA NDC Directory

Product NDC (as listed)66096-757Labeler and product segments. Claims need a package NDC.

Product NDC at billing width66096-0757Add 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
66096-757-02	66096075702	30 mL in 1 BOTTLE, SPRAY (66096-757-02)Marketed from Dec 19, 2018

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): Ohm-Inma
Generic name (nonproprietary): aconitum napellus, aranea diadema, arnica montana, asclepias vincetoxicum, baptisia tinctoria, bryonia alba, echinacea angustifolia, equisetum hyemale, eupatorium perforliatum, gelsemium sempervirens, hepar sulphuris calcareum, juglans regia, phytolacca decandra, sanguinaria canadensis, sarsaparilla, sulphur, zincum metallicum
Active ingredients: Aconitum napellus — 7 [hp_X]/30mLAraneus diadematus — 9 [hp_X]/30mLArnica montana — 6 [hp_X]/30mLCynanchum vincetoxicum root — 12 [hp_X]/30mLBaptisia tinctoria — 8 [hp_X]/30mLBryonia alba root — 10 [hp_X]/30mLEchinacea angustifolia — 6 [hp_X]/30mLEquisetum hyemale — 7 [hp_X]/30mLEupatorium perfoliatum flowering top — 10 [hp_X]/30mLGelsemium sempervirens root — 8 [hp_X]/30mLCalcium sulfide — 12 [hp_X]/30mLJuglans regia leaf — 6 [hp_X]/30mLPhytolacca americana root — 10 [hp_X]/30mLSanguinaria canadensis root — 8 [hp_X]/30mLSarsaparilla — 9 [hp_X]/30mLSulfur — 10 [hp_X]/30mLZinc — 12 [hp_X]/30mL
Dosage form: Spray
Route: Oral
Labeler: OHM PHARMA INC.
Product type: Prescription drug
Marketing category: Unapproved homeopathic
Marketing start: Dec 19, 2018
Listing expires: Dec 31, 2026
Identifiers: Product ID 66096-757_132d6703-451f-4dca-b1bc-997c667354d1SPL ID 132d6703-451f-4dca-b1bc-997c667354d1SPL set ID bc8e72c7-b7e6-4d5d-bd37-75202244d440UNII U0NQ8555JD, 6T6CO7R3Z5, O80TY208ZW, 9R858U917W, 5K1UO2888Y, T7J046YI2B, VB06AV5US8, 59677RXH25, 1W0775VX6E, 639KR60Q1Q, 1MBW07J51Q, 85HKB87105, 11E6VI8VEG, N9288CD508, 2H1576D5WG, 70FD1KFU70, J41CSQ7QDS

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

N466096075702 followed by a unit qualifier and the quantity

Package 66096-0757-02. 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 Mar 25, 2021.

Indications (excerpt from the label)

Contraindicaciones: Ninguna reportada

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)