Anti-Wart NDC 62106-1238

NDC codes

FDA NDC Directory

Product NDC (as listed)62106-1238Labeler and product segments. Claims need a package NDC.

Product NDC at billing width62106-1238Add 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
62106-1238-8	62106123808	1 BOTTLE, GLASS in 1 CARTON (62106-1238-8) / 20 mL in 1 BOTTLE, GLASSMarketed from Apr 3, 2017

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-Wart
Generic name (nonproprietary): bufo rana, buxus sempervirens, juglans regia, nitricum acidum, oleander, stannum metallicum, sulphur, taxus baccata, thuja occidentalis, vanadium metallicum
Active ingredients: Tin — 10 [hp_X]/20mLEnglish walnut — 2 [hp_X]/20mLNerium oleander leaf — 6 [hp_X]/20mLBufo bufo cutaneous gland — 12 [hp_X]/20mLNitric acid — 10 [hp_X]/20mLSulfur — 10 [hp_X]/20mLThuja occidentalis leafy twig — 8 [hp_X]/20mLVanadium — 10 [hp_X]/20mLBuxus sempervirens leafy twig — 6 [hp_X]/20mLTaxus baccata whole — 6 [hp_X]/20mL
Dosage form: Liquid
Route: Oral
Labeler: Seroyal USA
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Apr 3, 2017
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Nut Proteins (EXT)
Identifiers: Product ID 62106-1238_ed11e5b0-cdb5-1f9a-e053-2995a90a0f16SPL ID ed11e5b0-cdb5-1f9a-e053-2995a90a0f16SPL set ID 4c45c2e7-e4b7-0a93-e054-00144ff8d46cUNII 387GMG9FH5, 1V3SHR7QB7, 7KV510R6H6, Q59QU6N72Q, 411VRN1TV4, 70FD1KFU70, 1NT28V9397, 00J9J9XKDE, L479H0RS38, T0311VH21D
Pharmacologic class: Non-Standardized Food 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

N462106123808 followed by a unit qualifier and the quantity

Package 62106-1238-08. 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 9, 2022.

Indications (excerpt from the label)

Uses For the temporary relief of symptoms associated with skin warts. Directions To be taken ten minutes away from food. Invert bottle and shake lightly allowing drops to fall directly under the tongue or into ¼ oz of water. Hold contents for about 20 seconds and swallow. To promote drop flow, invert bottle and shake before each use. Adults and adolescents (12 years and older) Take 10 drops two times daily, in the morning and evening, or as recommended by your healthcare practitioner. Children (under 12 years) Take under the direction of your healthcare practitioner.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)