Bestmade Natural Products Thuja Occ NDC 82969-5100

NDC codes

FDA NDC Directory

Product NDC (as listed)82969-5100Labeler and product segments. Claims need a package NDC.

Product NDC at billing width82969-5100Add 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
82969-5100-1	82969510001	30 [hp_C] in 1 BOTTLE, GLASS (82969-5100-1)Marketed from Jan 1, 2015

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): Bestmade Natural Products Thuja Occ
Generic name (nonproprietary): thuja occidentalis
Active ingredients: Thuja occidentalis leafy twig — 30 [hp_C]/30[hp_C]
Dosage form: Tablet, Soluble
Route: Oral
Labeler: Bestmade Natural Products
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jan 1, 2015
Listing expires: Dec 31, 2026
Identifiers: Product ID 82969-5100_2fac50b2-a7c8-402b-e063-6294a90a96baSPL ID 2fac50b2-a7c8-402b-e063-6294a90a96baSPL set ID 2fac50b2-a7c7-402b-e063-6294a90a96baUNII 1NT28V9397

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

N482969510001 followed by a unit qualifier and the quantity

Package 82969-5100-01. 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 Mar 6, 2025.

Indications (excerpt from the label)

Uses Temporarily relieves discomfort due to oily skin, dry skin, sensitive or itchy eruptions, and nail fungus.* *CLAIMS BASED ON TRADITIONAL HOMEOPATHIC PRACTICE, NOT ACCEPTED MEDICAL EVIDENCE. NOT FDA EVALUATED. This product is not intended to diagnose, treat, cure, or prevent any disease.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)