Chemicals NDC 50845-0250

NDC codes

FDA NDC Directory

Product NDC (as listed)50845-0250Labeler and product segments. Claims need a package NDC.

Product NDC at billing width50845-0250Add 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
50845-0250-1	50845025001	30 mL in 1 BOTTLE, SPRAY (50845-0250-1)Marketed from Mar 25, 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): Chemicals
Generic name (nonproprietary): carduus marianus, hepar suis, lung suis, nux vomica, pancreas suis, phosphorus, serum anguillae, terebinthina, x-ray, zingiber officinale
Active ingredients: Silybum marianum seed — 3 [hp_X]/mLPork liver — 6 [hp_X]/mLSus scrofa lung — 6 [hp_X]/mLStrychnos nux-vomica seed — 200 [hp_C]/mLSus scrofa pancreas — 6 [hp_X]/mLPhosphorus — 200 [hp_C]/mLAnguilla rostrata blood serum — 30 [hp_C]/mLTurpentine oil — 6 [hp_X]/mLAlcohol, X-ray exposed (1000 rad) — 200 [hp_C]/mLGinger — 6 [hp_X]/mL
Dosage form: Spray
Route: Oral
Labeler: Liddell Laboratories, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Mar 25, 2019
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Food Additives (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 50845-0250_67d05c71-dbcd-4141-ba1d-eec23beafd2eSPL ID 67d05c71-dbcd-4141-ba1d-eec23beafd2eSPL set ID 7f241c5c-125a-414b-9549-9b1a7fc21defUNII U946SH95EE, 6EC706HI7F, 7GL3G1COB3, 269XH13919, 9Y3J3362RY, 27YLU75U4W, L7B16ESD1U, C5H0QJ6V7F, 6PRJ93602P, C5529G5JPQUPC 0363113264968
Pharmacologic class: Non-Standardized Food Allergenic Extract; Non-Standardized Plant 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

N450845025001 followed by a unit qualifier and the quantity

Package 50845-0250-01. 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 Jun 22, 2023.

Indications (excerpt from the label)

USES: May help detoxify from household and industrial chemicals. May temporarily relieve associated symptoms: • fatigue • dizziness • weakness • headache • poor concentration • dry skin** **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)