NDC codes

FDA NDC Directory
Product NDC (as listed)50845-0265Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50845-0265Add 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
50845-0265-1508450265015084502650130 mL in 1 BOTTLE, SPRAY (50845-0265-1)Marketed from Mar 26, 2020

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)
Pain
Generic name (nonproprietary)
aconitum napellus, arnica montana, bellis perennis, bryonia (alba), cartilago suis, causticum, chamomilla, coffea cruda, euphorbium officinarum, gnaphalium polycephalum, hypericum perforatum, magnesia phosphorica, passiflora incarnata, pyrogenium, ranunculus bulbosus, symphytum officinale
Active ingredients
Aconitum napellus whole — 200 [hp_C]/mLArnica montana whole — 3 [hp_X]/mLBellis perennis whole — 3 [hp_X]/mLBryonia alba root — 12 [hp_X]/mLSus scrofa cartilage — 6 [hp_X]/mLCausticum — 200 [hp_C]/mLMatricaria chamomilla whole — 3 [hp_X]/mLArabica coffee bean — 200 [hp_C]/mLEuphorbia resinifera resin — 6 [hp_X]/mLPseudognaphalium obtusifolium whole — 3 [hp_X]/mLHypericum perforatum whole — 200 [hp_C]/mLMagnesium phosphate, Dibasic trihydrate — 12 [hp_X]/mLPassiflora incarnata flowering top — 1 [hp_X]/mLRancid beef — 200 [hp_C]/mLRanunculus bulbosus whole — 6 [hp_X]/mLComfrey root — 6 [hp_X]/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
Other FDA classes
Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Small Intestine Fluid/Electrolyte Absorption (Physiologic effect)Magnesium Ion Exchange Activity (Mechanism)Osmotic Activity (Mechanism)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)
Identifiers
Product ID 50845-0265_98ae5431-1b62-4394-a9b9-cb8c45f674f2SPL ID 98ae5431-1b62-4394-a9b9-cb8c45f674f2SPL set ID b591e679-b481-47f1-8d4e-3f3040e9a42aUNII U0NQ8555JD, O80TY208ZW, 2HU33I03UY, T7J046YI2B, 73ECW5WG2F, DD5FO1WKFU, G0R4UBI2ZZ, 3SW678MX72, 1TI1O9028K, 36XQ854NWW, XK4IUX8MNB, HF539G9L3Q, CLF5YFS11O, 29SUH5R3HU, AEQ8NXJ0MB, M9VVZ08EKQUPC 0363113231960
Pharmacologic class
Calculi Dissolution Agent; Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract; Osmotic Laxative

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

N450845026501 followed by a unit qualifier and the quantity

Package 50845-0265-01. 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 relieve minor aches and pains.** **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 50845-0265

What is NDC 50845-0265?
50845-0265 is the product NDC for Pain, Aconitum napellus whole 200 [hp_C]/mL + 15 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?
Pain (Aconitum Napellus, Arnica Montana, Bellis Perennis, Bryonia (Alba), Cartilago Suis, Causticum, Chamomilla, Coffea Cruda, Euphorbium Officinarum, Gnaphalium Polycephalum, Hypericum Perforatum, Magnesia Phosphorica, Passiflora Incarnata, Pyrogenium, Ranunculus Bulbosus, Symphytum Officinale).
What is the active ingredient?
Aconitum napellus whole, Arnica montana whole, Bellis perennis whole, Bryonia alba root, Sus scrofa cartilage, Causticum, Matricaria chamomilla whole, Arabica coffee bean, Euphorbia resinifera resin, Pseudognaphalium obtusifolium whole, Hypericum perforatum whole, Magnesium phosphate, Dibasic trihydrate, Passiflora incarnata flowering top, Rancid beef, Ranunculus bulbosus whole, Comfrey root.
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 Pain?
1 other product NDC are listed under this name. See all Pain NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Pain NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Painreuseable painMethyl salicylate 10 g/1001 + 2 more ingredientsPatchTopicalShenzhen Mengyue Technology Co., Ltd.87255-00587255-0005-0187255-0005-02

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