Sepia Plex NDC 62106-0117

NDC codes

FDA NDC Directory

Product NDC (as listed)62106-0117Labeler and product segments. Claims need a package NDC.

Product NDC at billing width62106-0117Add 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
62106-0117-0	62106011700	1 BOTTLE, GLASS in 1 CARTON (62106-0117-0) / 30 mL in 1 BOTTLE, GLASSMarketed from Apr 3, 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): Sepia Plex
Generic name (nonproprietary): aconitum napellus, cimicifuga racemosa, lachesis mutus, melissa officinalis, platinum metallicum, sanguinaria canadensis, sepia, sulphuricum acidum, valeriana officinalis
Active ingredients: Black cohosh — 3 [hp_X]/30mLLachesis muta venom — 8 [hp_X]/30mLPlatinum — 8 [hp_X]/30mLSanguinaria canadensis root — 3 [hp_X]/30mLSepia officinalis juice — 3 [hp_X]/30mLMelissa officinalis — 2 [hp_X]/30mLSulfuric acid — 6 [hp_X]/30mLValerian — 6 [hp_X]/30mLAconitum napellus — 6 [hp_X]/30mL
Dosage form: Liquid
Route: Oral
Labeler: Seroyal USA
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Apr 3, 2017
Listing expires: Dec 31, 2026
Identifiers: Product ID 62106-0117_c72dc8a8-5a42-fb8c-e053-2a95a90a9e5fSPL ID c72dc8a8-5a42-fb8c-e053-2a95a90a9e5fSPL set ID 4c4a0a95-3848-4e19-e054-00144ff8d46cUNII K73E24S6X9, VSW71SS07I, 49DFR088MY, N9288CD508, QDL83WN8C2, YF70189L0N, O40UQP6WCF, JWF5YAW3QW, U0NQ8555JD

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

N462106011700 followed by a unit qualifier and the quantity

Package 62106-0117-00. 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 For the temporary relief of symptoms associated with menopause. 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: Take 10 drops three times daily or as recommended by your healthcare practitioner.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)