Unda 295 NDC 62106-1168

NDC codes

FDA NDC Directory

Product NDC (as listed)62106-1168Labeler and product segments. Claims need a package NDC.

Product NDC at billing width62106-1168Add 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
62106-1168-8	62106116808	1 BOTTLE, GLASS in 1 CARTON (62106-1168-8) / 20 mL in 1 BOTTLE, GLASSMarketed from May 27, 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 295
Generic name (nonproprietary): pulsatilla, nux vomica, aloe socotrina
Active ingredients: Strychnos nux-vomica seed — 4 [hp_X]/20mLAloe — 6 [hp_X]/20mLPulsatilla vulgaris — 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 27, 2015
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 62106-1168_ebe194aa-984d-8373-e053-2995a90ae03eSPL ID ebe194aa-984d-8373-e053-2995a90ae03eSPL set ID 079c945e-7853-3410-e054-00144ff88e88UNII 52JDS841PX, I76KB35JEV, 6D74QW4H67, O84B5194RL, 269XH13919, 8L72OKJ7II, JWF5YAW3QW, 1TH8Q20J0U, W2FH8O2BBE, YF70189L0N, G3QC02NIE6, CLF5YFS11O, W0X9457M59, 3M4G523W1G, X621621QQV, B4R1EZ1R1D, V5VD430YW9, 1WZA4Y92EX, S2D77IH61R, 79M2M2UDA9, 79Y1949PYO, 2P299V784P, Z1EJP3037Z, AK7JF626KX
Pharmacologic class: 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

N462106116808 followed by a unit qualifier and the quantity

Package 62106-1168-08. 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 Oct 25, 2022.

Indications (excerpt from the label)

Uses For the temporary relief of symptoms associated with minor 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)