What is NDC 50845-0280?

50845-0280 is the product NDC for Derma Pain, Calendula officinalis flowering top 12 [hp_X]/mL + 5 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?

Derma Pain (Calendula Officinalis, Croton Tiglium, Natrum Muriaticum, Plantago Major, Rhus Tox, Sarsaparilla (Smilax Regelii)).

What is the active ingredient?

Calendula officinalis flowering top, Croton tiglium seed, Sodium chloride, Plantago major whole, Toxicodendron pubescens leaf, Smilax ornata root.

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 Derma Pain?

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.

Derma Pain NDC 50845-0280 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)50845-0280Labeler and product segments. Claims need a package NDC.

Product NDC at billing width50845-0280Add 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
50845-0280-1	5084502800150845028001	30 mL in 1 BOTTLE, SPRAY (50845-0280-1)Marketed from Jun 29, 2022

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): Derma Pain
Generic name (nonproprietary): calendula officinalis, croton tiglium, natrum muriaticum, plantago major, rhus tox, sarsaparilla (smilax regelii)
Active ingredients: Calendula officinalis flowering top — 12 [hp_X]/mLCroton tiglium seed — 30 [hp_X]/mLSodium chloride — 30 [hp_X]/mLPlantago major whole — 30 [hp_X]/mLToxicodendron pubescens leaf — 30 [hp_X]/mLSmilax ornata root — 30 [hp_X]/mL
Dosage form: Spray
Route: Topical
Labeler: Liddell Laboratories, Inc.NDC labeler code 50845
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jun 29, 2022
Marketing end: Mar 9, 2027
Identifiers: Product ID 50845-0280_f378a799-7c5f-45bf-a78b-1f9617f30121SPL ID f378a799-7c5f-45bf-a78b-1f9617f30121SPL set ID e02a5e99-aa27-4276-a785-7b5328d89fdcUNII 18E7415PXQ, 0HK2GZK66E, 451W47IQ8X, W2469WNO6U, 6IO182RP7A, 2H1576D5WGUPC 0363113336993

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. Topical products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N450845028001 followed by a unit qualifier and the quantity

Package 50845-0280-01. 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 Nov 4, 2024.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve shooting pain, itching, burning, and sensitivity to touch, with or after eruptions and blisters.** **Clains 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 50845-0280

What is NDC 50845-0280?: 50845-0280 is the product NDC for Derma Pain, Calendula officinalis flowering top 12 [hp_X]/mL + 5 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?: Derma Pain (Calendula Officinalis, Croton Tiglium, Natrum Muriaticum, Plantago Major, Rhus Tox, Sarsaparilla (Smilax Regelii)).
What is the active ingredient?: Calendula officinalis flowering top, Croton tiglium seed, Sodium chloride, Plantago major whole, Toxicodendron pubescens leaf, Smilax ornata 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 Derma Pain?: 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.