NDC codes

FDA NDC Directory
Product NDC (as listed)50845-0237Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50845-0237Add 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
50845-0237-1508450237015084502370130 mL in 1 BOTTLE, SPRAY (50845-0237-1)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)
Back Pain and Sciatica
Generic name (nonproprietary)
aconitum napellus, arnica montana, belladonna, cimicifuga racemosa, euphorbium officinarum, gelsemium sempervirens, gnaphalium polycephalum, hypericum perforatum, magnesia phosphorica, phytolacca decandra, ranunculus bulbosus, rhus tox
Active ingredients
Aconitum napellus whole — 200 [hp_C]/mLArnica montana whole — 200 [hp_C]/mLAtropa belladonna — 6 [hp_X]/mLBlack cohosh — 6 [hp_X]/mLEuphorbia resinifera resin — 6 [hp_X]/mLGelsemium sempervirens root — 6 [hp_X]/mLPseudognaphalium obtusifolium whole — 30 [hp_X]/mLHypericum perforatum whole — 200 [hp_C]/mLMagnesium phosphate, Dibasic trihydrate — 10 [hp_X]/mLPhytolacca americana root — 4 [hp_X]/mLRanunculus bulbosus whole — 30 [hp_C]/mLToxicodendron pubescens leaf — 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
Other FDA classes
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)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)
Identifiers
Product ID 50845-0237_d340d01b-3f0f-4863-a0b0-94cff53d2215SPL ID d340d01b-3f0f-4863-a0b0-94cff53d2215SPL set ID 2ae11146-b869-4a53-afa3-805de12921f9UNII U0NQ8555JD, O80TY208ZW, WQZ3G9PF0H, K73E24S6X9, 1TI1O9028K, 639KR60Q1Q, 36XQ854NWW, XK4IUX8MNB, HF539G9L3Q, 11E6VI8VEG, AEQ8NXJ0MB, 6IO182RP7A
Pharmacologic class
Calculi Dissolution Agent; 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

N450845023701 followed by a unit qualifier and the quantity

Package 50845-0237-01. 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 these symptoms of back pain and sciatica: lower back pain muscle cramps neck and back stiffness muscle spasms** **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 50845-0237

What is NDC 50845-0237?
50845-0237 is the product NDC for Back Pain and Sciatica, Aconitum napellus whole 200 [hp_C]/mL + 11 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?
Back Pain and Sciatica (Aconitum Napellus, Arnica Montana, Belladonna, Cimicifuga Racemosa, Euphorbium Officinarum, Gelsemium Sempervirens, Gnaphalium Polycephalum, Hypericum Perforatum, Magnesia Phosphorica, Phytolacca Decandra, Ranunculus Bulbosus, Rhus Tox).
What is the active ingredient?
Aconitum napellus whole, Arnica montana whole, Atropa belladonna, Black cohosh, Euphorbia resinifera resin, Gelsemium sempervirens root, Pseudognaphalium obtusifolium whole, Hypericum perforatum whole, Magnesium phosphate, Dibasic trihydrate, Phytolacca americana root, Ranunculus bulbosus whole, Toxicodendron pubescens leaf.
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 Back Pain and Sciatica?
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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