Anti-Scar Drops 2084 (anti-scar drops) NDC 63083-2084

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-2084Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-2084Add 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
63083-2084-2	63083208402	59 mL in 1 BOTTLE, DROPPER (63083-2084-2)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): Anti-Scar Drops 2084Suffix: 2084
Generic name (nonproprietary): anti-scar drops
Active ingredients: Thuja occidentalis leaf — 3 [hp_X]/59mLAconitum napellus whole — 6 [hp_X]/59mLPotassium alum — 6 [hp_X]/59mLSilicon dioxide — 6 [hp_X]/59mLAnhydrous dibasic calcium phosphate — 6 [hp_X]/59mLAllylthiourea — 6 [hp_X]/59mLNitric acid — 8 [hp_X]/59mLGraphite — 12 [hp_X]/59mLLactose, X-ray exposed (1000 rad) — 60 [hp_X]/59mLArnica montana whole — 100 [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
Identifiers: Product ID 63083-2084_e82549c8-f10f-4e84-b444-e58e5eb195dfSPL ID e82549c8-f10f-4e84-b444-e58e5eb195dfSPL set ID ad0e9159-ed68-48aa-a7d1-7ff5c32ec304UNII 0T0DQN8786, U0NQ8555JD, 1L24V9R23S, ETJ7Z6XBU4, L11K75P92J, 706IDJ14B7, 411VRN1TV4, 4QQN74LH4O, LNT739I158, O80TY208ZW

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

N463083208402 followed by a unit qualifier and the quantity

Package 63083-2084-02. 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 painful, sensitive, or itchy skin resulting from injury.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)