Unda 22 NDC 62106-1121

NDC codes

FDA NDC Directory

Product NDC (as listed)62106-1121Labeler and product segments. Claims need a package NDC.

Product NDC at billing width62106-1121Add 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
62106-1121-8	62106112108	1 BOTTLE, GLASS in 1 CARTON (62106-1121-8) / 20 mL in 1 BOTTLE, GLASSMarketed from Sep 21, 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 22
Generic name (nonproprietary): absinthium, aconitum napellus, argentum metallicum, boldo leaf, chamomilla, coffea tosta, jateorhiza palmata, manganum oxydatum nigrum, salvia officinalis
Active ingredients: Manganese dioxide — 12 [hp_X]/20mLSage — 4 [hp_X]/20mLPeumus boldus leaf — 4 [hp_X]/20mLMatricaria recutita — 4 [hp_X]/20mLJateorhiza calumba root — 4 [hp_X]/20mLWormwood — 4 [hp_X]/20mLAconitum napellus — 4 [hp_X]/20mLSilver — 12 [hp_X]/20mLCoffea arabica seed, Roasted — 4 [hp_X]/20mL
Dosage form: Liquid
Route: Oral
Labeler: Seroyal USA
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Sep 21, 2015
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)Plant Proteins (Chemical structure)
Identifiers: Product ID 62106-1121_c732aeb0-c867-9e33-e053-2a95a90a129eSPL ID c732aeb0-c867-9e33-e053-2a95a90a129eSPL set ID 2044a04e-275f-3f16-e054-00144ff8d46cUNII 9H58JRT35E, V36I2B8LD5, F84709P2XV, 387GMG9FH5, U0NQ8555JD, CK15HA8438, B10M69172N, 75O014T1HG, M7T6H7D4IF, 997724QNDS, 065C5D077J, G0R4UBI2ZZ, 597E9BI3Z3, 00543AP1JV, 9Q24RAI43V, JWF5YAW3QW, BJ7YPN79A1, F79059A38U, PB618V0K2W, 3M4G523W1G, 639KR60Q1Q, KPS1B1162N, 2H1576D5WG, RV23PE6426, Q4EWM09M3O, 79M2M2UDA9, IH3063S9MY, 79Y1949PYO, Q21UUL2105, TF219GU161
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

N462106112108 followed by a unit qualifier and the quantity

Package 62106-1121-08. 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 Jul 15, 2021.

Indications (excerpt from the label)

Uses For the temporary relief of symptoms associated with mild skin irritation. 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)