NDC codes

FDA NDC Directory
Product NDC (as listed)50845-0248Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50845-0248Add 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
50845-0248-1508450248015084502480130 mL in 1 BOTTLE, SPRAY (50845-0248-1)Marketed from Jan 30, 2019

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)
Emf
Generic name (nonproprietary)
argentum nitricum, arnica montana, baptisia tinctoria, cinchona officinalis, galium aparine, hepar suis, natrum carbonicum, panax ginseng, phosphoricum acidum, phosphorus, rhododendron chrysanthum, strontium carbonicum, sulphur iodatum, thuja occidentalis, x-ray
Active ingredients
Silver nitrate — 30 [hp_C]/mLArnica montana whole — 3 [hp_X]/mLBaptisia tinctoria root — 3 [hp_X]/mLCinchona officinalis bark — 6 [hp_X]/mLGalium aparine whole — 3 [hp_X]/mLPork liver — 6 [hp_X]/mLSodium carbonate — 200 [hp_C]/mLAsian ginseng — 1 [hp_X]/mLPhosphoric acid — 3 [hp_X]/mLPhosphorus — 12 [hp_X]/mLRhododendron aureum leaf — 30 [hp_C]/mLStrontium carbonate — 12 [hp_X]/mLSulfur iodide — 200 [hp_C]/mLThuja occidentalis leafy twig — 200 [hp_C]/mLAlcohol, X-ray exposed (1000 rad) — 200 [hp_C]/mL
Dosage form
Spray
Route
Oral
Labeler
Liddell Laboratories, Inc.NDC labeler code 50845
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Listing expires
Identifiers
Product ID 50845-0248_a12452f8-d7ea-4e84-b827-7483e69b5f48SPL ID a12452f8-d7ea-4e84-b827-7483e69b5f48SPL set ID 3fa1b8d3-7c09-431b-b843-03b2ef8a92b1UNII 95IT3W8JZE, O80TY208ZW, 5EF0HWI5WU, S003A158SB, Z4B6561488, 6EC706HI7F, 45P3261C7T, CUQ3A77YXI, E4GA8884NN, 27YLU75U4W, IV92NQJ73U, 41YPU4MMCA, L6L8KA2AA0, 1NT28V9397, 6PRJ93602P

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

N450845024801 followed by a unit qualifier and the quantity

Package 50845-0248-01. 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 .

Indications (excerpt from the label)

INDICATIONS: May temporarily aid in detoxifying the body and temporarily relieve symptoms of electromagnetic field (EMF) radiation exposure, such as: recurring fatigue nausea disturbed sleep frequent headaches mental confusion** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 50845-0248

What is NDC 50845-0248?
50845-0248 is the product NDC for Emf, Silver nitrate 30 [hp_C]/mL + 14 more ingredients spray, listed with the FDA by Liddell Laboratories, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Emf (Argentum nitricum, Arnica montana, Baptisia tinctoria, Cinchona officinalis, Galium aparine, Hepar suis, Natrum carbonicum, Panax ginseng, Phosphoricum acidum, Phosphorus, Rhododendron Chrysanthum, Strontium Carbonicum, Sulphur iodatum, Thuja occidentalis, X-ray).
What is the active ingredient?
Silver nitrate, Arnica montana whole, Baptisia tinctoria root, Cinchona officinalis bark, Galium aparine whole, Pork liver, Sodium carbonate, Asian ginseng, Phosphoric acid, Phosphorus, Rhododendron aureum leaf, Strontium carbonate, Sulfur iodide, Thuja occidentalis leafy twig, Alcohol, X-ray exposed (1000 rad).
Who is the labeler?
Liddell Laboratories, Inc., NDC labeler code 50845. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Emf?
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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