Unda 41 NDC 62106-1140

NDC codes

FDA NDC Directory

Product NDC (as listed)62106-1140Labeler and product segments. Claims need a package NDC.

Product NDC at billing width62106-1140Add 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
62106-1140-8	62106114008	1 BOTTLE, GLASS in 1 CARTON (62106-1140-8) / 20 mL in 1 BOTTLE, GLASSMarketed from May 26, 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): Unda 41
Generic name (nonproprietary): primula veris, rheum, juglans regia, sarsaparilla, nux vomica, symphytum officinale, plumbum metallicum
Active ingredients: Sarsaparilla — 4 [hp_X]/20mLPrimula veris — 4 [hp_X]/20mLStrychnos nux-vomica seed — 4 [hp_X]/20mLComfrey root — 6 [hp_X]/20mLLead — 12 [hp_X]/20mLRheum tanguticum whole — 4 [hp_X]/20mLEnglish walnut — 4 [hp_X]/20mL
Dosage form: Liquid
Route: Oral
Labeler: Seroyal USA
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: May 26, 2015
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)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Nut Proteins (EXT)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 62106-1140_ddbf25ea-80d2-5725-e053-2a95a90abaccSPL ID ddbf25ea-80d2-5725-e053-2a95a90abaccSPL set ID 16ee1833-db7c-46fe-e054-00144ff88e88UNII 789U1901C5, 3M4G523W1G, 8L72OKJ7II, S546YLW6E6, 492225Q21H, 654825W09Z, 2H1576D5WG, QH89N6B02U, E55SMD6DA8, 79Y1949PYO, IHN2NQ5OF9, S7V92P67HO, W6LFQ57E4M, 26ZE1BZ2US, 1NT28V9397, 00UK7646FG, CPD4NFA903, AWN2M136UL, 18E7415PXQ, ZW3Z11D0JV, 269XH13919, M9VVZ08EKQ, 7TPC058OWY, 0R715588D2, N20HL7Q941, 1V3SHR7QB7, 2P299V784PUPC 0883196301607, 0883196305605
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

N462106114008 followed by a unit qualifier and the quantity

Package 62106-1140-08. 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 Apr 28, 2022.

Indications (excerpt from the label)

Uses For the temporary relief of mild fever. Directions Adults and adolescents (12 years and older) Take 5 drops three times daily 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)