Drosera Plex (cough syrup) NDC 62106-3126

NDC codes

FDA NDC Directory

Product NDC (as listed)62106-3126Labeler and product segments. Claims need a package NDC.

Product NDC at billing width62106-3126Add 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
62106-3126-1	62106312601	1 BOTTLE, GLASS in 1 CARTON (62106-3126-1) / 180 mL in 1 BOTTLE, GLASSMarketed from Sep 6, 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): Drosera Plex
Generic name (nonproprietary): cough syrup
Active ingredients: Pulsatilla pratensis — 8 [hp_X]/180mLSpongia officinalis skeleton, Roasted — 10 [hp_X]/180mLHyoscyamus niger — 10 [hp_X]/180mLLachesis muta venom — 10 [hp_X]/180mLPapaver rhoeas flower — 5 [hp_X]/180mLDrosera rotundifolia — 3 [hp_X]/180mLOregano flowering top — 7 [hp_X]/180mLSulfur — 8 [hp_X]/180mLIpecac — 6 [hp_X]/180mLRumex crispus root — 10 [hp_X]/180mL
Dosage form: Syrup
Route: Oral
Labeler: Seroyal USA
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Sep 6, 2017
Listing expires: Dec 31, 2026
Identifiers: Product ID 62106-3126_ed11ed9c-1d4f-d766-e053-2a95a90aa977SPL ID ed11ed9c-1d4f-d766-e053-2a95a90aa977SPL set ID 588871b1-1dae-3053-e053-2a91aa0a8124UNII 8E272251DI, 1PIP394IID, 4WRK2153H3, VSW71SS07I, Y1MLS7E68X, QR44N9XPJQ, 7K91ZBK8GJ, 70FD1KFU70, 62I3C8233L, 9N1RM2S62C

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

N462106312601 followed by a unit qualifier and the quantity

Package 62106-3126-01. 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 temporary cough relief. Directions Adults Take 1 tablespoon (15 ml) three to five times daily, or as recommended by your healthcare practitioner. Children (over 2 years) Take 1 teaspoon (5 ml) three to five times daily, or as recommended by your healthcare practitioner. Children (under 2 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)