Sulphur Remedy NDC 43742-0745

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-0745Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-0745Add 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
43742-0745-1	43742074501	30 mL in 1 BOTTLE, DROPPER (43742-0745-1)Marketed from May 4, 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): Sulphur Remedy
Generic name (nonproprietary): sulphur, asclepias tuberosa, bryonia, dulcamara
Active ingredients: Sulfur — 4 [hp_X]/mLAsclepias tuberosa root — 6 [hp_X]/mLBryonia alba root — 10 [hp_X]/mLSolanum dulcamara stem — 10 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Deseret Biologicals, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: May 4, 2016
Listing expires: Dec 31, 2026
Identifiers: Product ID 43742-0745_329b8913-d3b6-4d30-a089-215c3f2cdc49SPL ID 329b8913-d3b6-4d30-a089-215c3f2cdc49SPL set ID a77ef404-a836-4c3a-830f-bfe22127990fUNII 70FD1KFU70, 1ZL82U5D18, T7J046YI2B, IR986LE7DFUPC 0810151881171

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

N443742074501 followed by a unit qualifier and the quantity

Package 43742-0745-01. 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 Oct 23, 2024.

Indications (excerpt from the label)

USES: • For the temporary relief of symptoms including: • headache • fever • muscle aches • skin inflammation 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)