Ver NDC 43742-2043

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-2043Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-2043Add 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
43742-2043-1	43742204301	60 mL in 1 BOTTLE, DROPPER (43742-2043-1)Marketed from Mar 10, 2023

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): Ver
Generic name (nonproprietary): artemisia vulgaris, ascaris lumbricoides, brugia malayi, calcarea carbonica, cina, cryptosporidium parvum, enterobius vermicularis, filix mas, giardia lamblia, graphites, iodium, mercurius corrosivus, quassia (amara), sabadilla, silicea, spigelia anthelmia, taenia saginata, taenia solium, teucrium marum, thymus serpyllum, trichinella spiralis, trichomonas vaginalis
Active ingredients: Artemisia vulgaris root — 2 [hp_X]/mLAscaris lumbricoides — 15 [hp_X]/mLBrugia malayi — 39 [hp_C]/mLOyster shell calcium carbonate, Crude — 12 [hp_X]/mLArtemisia cina pre-flowering top — 8 [hp_X]/mLCryptosporidium parvum — 20 [hp_C]/mLEnterobius vermicularis — 33 [hp_X]/mLDryopteris filix-mas root — 7 [hp_X]/mLGiardia lamblia — 18 [hp_C]/mLGraphite — 12 [hp_X]/mLIodine — 12 [hp_X]/mLMercuric chloride — 12 [hp_X]/mLQuassia amara wood — 3 [hp_X]/mLSchoenocaulon officinale seed — 12 [hp_X]/mLSilicon dioxide — 8 [hp_X]/mLSpigelia anthelmia whole — 8 [hp_X]/mLTaenia saginata — 20 [hp_C]/mLTaenia solium — 12 [hp_C]/mLTeucrium marum whole — 3 [hp_X]/mLThymus serpyllum whole — 3 [hp_X]/mLTrichinella spiralis — 15 [hp_X]/mLTrichomonas vaginalis — 13 [hp_C]/mL
Dosage form: Liquid
Route: Oral
Labeler: Deseret Biologicals, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Mar 10, 2023
Listing expires: Dec 31, 2026
Identifiers: Product ID 43742-2043_f373cfd2-847b-43aa-ace7-3f8864e6f2b5SPL ID f373cfd2-847b-43aa-ace7-3f8864e6f2b5SPL set ID b47bdd57-14cd-46e9-a34e-0d8a7c21bda2UNII 32MP823R8S, 5694HE17ZQ, V1NN02KTF0, 2E32821G6I, 28M1820ACT, TGR919EN5P, W1D68QW48M, C0ZK0RRF5X, 89IEJ09R73, 4QQN74LH4O, 9679TC07X4, 53GH7MZT1R, S5249Q85HW, 6NAF1689IO, ETJ7Z6XBU4, WYT05213GE, O27XH54AIC, 80CZ5Z3WH3, 10464S0TAA, 86H4S6K51N, 2PYI6D7HCQ, Q25X3G314LUPC 0810151884202

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

N443742204301 followed by a unit qualifier and the quantity

Package 43742-2043-01. 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 Mar 12, 2024.

Indications (excerpt from the label)

USES: • For the temporary relief of symptoms including: • vaginal discharge • stomach discomfort • flatulence • occasional diarrhea • intestinal spasms • occasional constipation These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)