Ohm-Dren Lft NDC 66096-754

NDC codes

FDA NDC Directory

Product NDC (as listed)66096-754Labeler and product segments. Claims need a package NDC.

Product NDC at billing width66096-0754Add 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
66096-754-02	66096075402	30 mL in 1 BOTTLE, SPRAY (66096-754-02)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-Dren Lft
Generic name (nonproprietary): apis mellifica, aranea diadema, berberis vulgaris, equisetum hyemale, galium aparine, juglans regia, manganum phosphoricum, nicotinamidum, nitricum acidum, sarsaparilla, thuja occidentalis, urtica urens
Active ingredients: Apis mellifera — 12 [hp_X]/30mLAraneus diadematus — 9 [hp_X]/30mLBerberis vulgaris root bark — 12 [hp_X]/30mLEquisetum hyemale — 7 [hp_X]/30mLGalium aparine — 6 [hp_X]/30mLJuglans regia whole — 6 [hp_X]/30mLManganese phosphate, Dibasic — 9 [hp_X]/30mLNiacinamide — 9 [hp_X]/30mLNitric acid — 12 [hp_X]/30mLSarsaparilla — 9 [hp_X]/30mLThuja occidentalis leafy twig — 6 [hp_X]/30mLUrtica urens — 6 [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
Other FDA classes: Allergens (Chemical structure)Bee Venoms (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Magnetic Resonance Contrast Activity (Mechanism)
Identifiers: Product ID 66096-754_b8a7d171-ccd8-16ea-e053-2a95a90a1100SPL ID b8a7d171-ccd8-16ea-e053-2a95a90a1100SPL set ID 31f4eaab-fbd6-4924-b956-c0ff2934fbf0UNII 7S82P3R43Z, 6T6CO7R3Z5, 1TH8Q20J0U, 59677RXH25, Z4B6561488, 87EJ76IO83, VZ3U1H7Q5B, 25X51I8RD4, 411VRN1TV4, 2H1576D5WG, 1NT28V9397, IHN2NQ5OF9
Pharmacologic class: Paramagnetic Contrast Agent; Standardized Insect Venom 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

N466096075402 followed by a unit qualifier and the quantity

Package 66096-0754-02. 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 Jan 11, 2021.

Indications (excerpt from the label)

USES: Temporarily relieves slow lymphatic drainage. Assists in removing toxins and improves metabolism.**

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)