Drosera Plex NDC 62106-1194

NDC codes

FDA NDC Directory

Product NDC (as listed)62106-1194Labeler and product segments. Claims need a package NDC.

Product NDC at billing width62106-1194Add 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
62106-1194-0	62106119400	1 BOTTLE, GLASS in 1 CARTON (62106-1194-0) / 30 mL in 1 BOTTLE, GLASSMarketed from Dec 14, 2016

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): Drosera Plex
Generic name (nonproprietary): arnica montana, belladonna, cina, coccus cacti, corallium rubrum, cuprum metallicum, drosera, ferrum phosphoricum, ipecacuanha, solidago virgaurea
Active ingredients: Copper — 6 [hp_X]/30mLArtemisia cina flower — 6 [hp_X]/30mLFerrum phosphoricum — 6 [hp_X]/30mLIpecac — 6 [hp_X]/30mLSolidago virgaurea flowering top — 2 [hp_X]/30mLDrosera rotundifolia flowering top — 6 [hp_X]/30mLAtropa belladonna whole — 6 [hp_X]/30mLArnica montana root — 6 [hp_X]/30mLProtortonia cacti — 6 [hp_X]/30mLCorallium rubrum exoskeleton — 6 [hp_X]/30mL
Dosage form: Liquid
Route: Sublingual
Labeler: Seroyal USA
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Dec 14, 2016
Listing expires: Dec 31, 2026
Other FDA classes: Copper (Chemical structure)Decreased Embryonic Implantation (Physiologic effect)Decreased Sperm Motility (Physiologic effect)Inhibit Ovum Fertilization (Physiologic effect)
Identifiers: Product ID 62106-1194_c72c4b1e-d849-9aa6-e053-2995a90ac5b2SPL ID c72c4b1e-d849-9aa6-e053-2995a90ac5b2SPL set ID 43a4b756-c80d-5043-e054-00144ff8d46cUNII 789U1901C5, 28M1820ACT, 91GQH8I5F7, 62I3C8233L, 5405K23S50, 75O014T1HG, DSV74G1P2J, MUE8Y11327, LZB7TFX1LT, 2CA71K0DLE
Pharmacologic class: Copper-containing Intrauterine Device

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. Sublingual products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N462106119400 followed by a unit qualifier and the quantity

Package 62106-1194-00. 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 Assists with the temporary relief of cough. 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. Dosage frequency may be increased up to six times daily depending on the severity of symptoms. Adults and adolescents (12 years and older) Take 10 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)