Low Back Pain Drops 2041 (low back pain drops) NDC 63083-2041

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-2041Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-2041Add 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
63083-2041-2	63083204102	59 mL in 1 BOTTLE, DROPPER (63083-2041-2)Marketed from Aug 15, 1985

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): Low Back Pain Drops 2041Suffix: 2041
Generic name (nonproprietary): low back pain drops
Active ingredients: Apis mellifera — 6 [hp_X]/59mLBerberis vulgaris root bark — 6 [hp_X]/59mLBos taurus hypothalamus — 6 [hp_X]/59mLPotassium dichromate — 6 [hp_X]/59mLBos taurus bone marrow — 6 [hp_X]/59mLLycopodium clavatum spore — 6 [hp_X]/59mLMagnesium phosphate, Dibasic trihydrate — 6 [hp_X]/59mLBos taurus somatic nerve — 6 [hp_X]/59mLSepia officinalis juice — 6 [hp_X]/59mLAconitum napellus whole — 6 [hp_X]/59mLAmaryllis belladonna whole — 6 [hp_X]/59mLCausticum — 6 [hp_X]/59mLToxicodendron pubescens leaf — 6 [hp_X]/59mLArnica montana whole — 6 [hp_X]/59mLAtropine — 12 [hp_X]/59mLGraphite — 12 [hp_X]/59mLHypericum perforatum whole — 30 [hp_X]/59mL
Dosage form: Liquid
Route: Oral
Labeler: Professional Complementary Health Formulas
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Aug 15, 1984
Listing expires: Dec 31, 2027
Other FDA classes: Allergens (Chemical structure)Bee Venoms (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cholinergic Antagonists (Mechanism)Cholinergic Muscarinic Antagonists (Mechanism)Increased Histamine Release (Physiologic effect)Increased IgG Production (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)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)
Identifiers: Product ID 63083-2041_c9c4d3b5-15e8-4c7c-963a-4a2c76dc048bSPL ID c9c4d3b5-15e8-4c7c-963a-4a2c76dc048bSPL set ID c9b3e606-5991-4ce4-9e0d-51bcb44da583UNII 7S82P3R43Z, 1TH8Q20J0U, S6G2NLH4Y7, T4423S18FM, 08X0K2M57P, C88X29Y479, HF539G9L3Q, N1R7LRU866, QDL83WN8C2, U0NQ8555JD, 11B89M58UN, DD5FO1WKFU, 6IO182RP7A, O80TY208ZW, 7C0697DR9I, 4QQN74LH4O, XK4IUX8MNB
Pharmacologic class: Anticholinergic; Calculi Dissolution Agent; Cholinergic Muscarinic Antagonist; Osmotic Laxative; 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

N463083204102 followed by a unit qualifier and the quantity

Package 63083-2041-02. 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 8, 2026.

Indications (excerpt from the label)

INDICATIONS For the temporary relief of minor pain or stiffness in the lower back.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)