NDC codes

FDA NDC Directory
Product NDC (as listed)66096-717Labeler and product segments. Claims need a package NDC.
Product NDC at billing width66096-0717Add 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 NDC11-digit (billing)PackageCopy
66096-717-02660960717026609607170230 mL in 1 BOTTLE, SPRAY (66096-717-02)Marketed from Feb 7, 2020

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-Anx
Generic name (nonproprietary)
argentum nitricum, aurum metallicum, avena sativa, gelsemium sempervirens, hyoscyamus niger, ignatia amara, moschus, natrum muriaticum, passiflora incarnata, stannum metallicum, valeriana officinalis
Active ingredients
Silver nitrate — 14 [hp_X]/30mLGold — 14 [hp_X]/30mLAvena sativa flowering top — 5 [hp_X]/30mLGelsemium sempervirens root — 14 [hp_X]/30mLHyoscyamus niger — 14 [hp_X]/30mLStrychnos ignatii seed — 14 [hp_X]/30mLMoschus moschiferus musk sac resin — 14 [hp_X]/30mLSodium chloride — 14 [hp_X]/30mLPassiflora incarnata flowering top — 5 [hp_X]/30mLTin — 16 [hp_X]/30mLValerian — 5 [hp_X]/30mL
Dosage form
Spray
Route
Oral
Labeler
OHM PHARMA INC.NDC labeler code 66096
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Listing expires
Other FDA classes
Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)
Identifiers
Product ID 66096-717_5ba1e4a9-baf1-4b73-8ff0-555089a9a4fdSPL ID 5ba1e4a9-baf1-4b73-8ff0-555089a9a4fdSPL set ID f743b690-8f79-4e60-81cd-e3e2825a1ec8UNII 95IT3W8JZE, 79Y1949PYO, MA9CQJ3F7F, 639KR60Q1Q, 4WRK2153H3, 1NM3M2487K, 8KFK4W7KP7, 451W47IQ8X, CLF5YFS11O, 387GMG9FH5, JWF5YAW3QW
Pharmacologic class
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

N466096071702 followed by a unit qualifier and the quantity

Package 66096-0717-02. 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 .

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)

About NDC 66096-717

What is NDC 66096-717?
66096-717 is the product NDC for Ohm-Anx, Silver nitrate 14 [hp_X]/30mL + 10 more ingredients spray, listed with the FDA by OHM PHARMA INC.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Ohm-Anx (Argentum Nitricum, Aurum Metallicum, Avena Sativa, Gelsemium Sempervirens, Hyoscyamus Niger, Ignatia Amara, Moschus, Natrum Muriaticum, Passiflora Incarnata, Stannum Metallicum, Valeriana Officinalis).
What is the active ingredient?
Silver nitrate, Gold, Avena sativa flowering top, Gelsemium sempervirens root, Hyoscyamus niger, Strychnos ignatii seed, Moschus moschiferus musk sac resin, Sodium chloride, Passiflora incarnata flowering top, Tin, Valerian.
Who is the labeler?
OHM PHARMA INC., NDC labeler code 66096. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Ohm-Anx?
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.

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