Back Pain and Sciatica NDC 50845-0237

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 NDC	11-digit (billing)	Package	Copy
50845-0237-1	50845023701	30 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.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jan 30, 2019
Listing expires: Dec 31, 2026
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 Jul 1, 2024.

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)