Multiple Miasm NDC 43742-0783

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-0783Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-0783Add 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
43742-0783-1	43742078301	30 mL in 1 BOTTLE, DROPPER (43742-0783-1)Marketed from Jun 27, 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): Multiple Miasm
Generic name (nonproprietary): arsenicum album, lycopodium clavatum, sulphur, aloe, carcinosin, nitricum acidum, silicea, thuja occidentalis
Active ingredients: Arsenic trioxide — 30 [hp_C]/mLLycopodium clavatum spore — 30 [hp_C]/mLSulfur — 30 [hp_C]/mLAloe — 30 [hp_C]/mLHuman breast tumor cell — 30 [hp_C]/mLNitric acid — 30 [hp_C]/mLSilicon dioxide — 30 [hp_C]/mLThuja occidentalis leaf — 30 [hp_C]/mL
Dosage form: Liquid
Route: Oral
Labeler: Deseret Biologicals, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jun 27, 2016
Marketing end: Dec 22, 2028
Identifiers: Product ID 43742-0783_8237a3f4-8966-4343-b5de-af29c734efb3SPL ID 8237a3f4-8966-4343-b5de-af29c734efb3SPL set ID 0cf54ec3-d731-4f27-89fd-4571d991a615UNII S7V92P67HO, C88X29Y479, 70FD1KFU70, V5VD430YW9, C62OO7VD9K, 411VRN1TV4, ETJ7Z6XBU4, 0T0DQN8786UPC 0810151881119

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

N443742078301 followed by a unit qualifier and the quantity

Package 43742-0783-01. 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 May 9, 2024.

Indications (excerpt from the label)

USES: • For the temporary relief of symptoms including: • miasmatic support • skin rashes • dry coughs • warts 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)