Bact Combination NDC 43742-2239

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-2239Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-2239Add 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
43742-2239-1	43742223901	30 mL in 1 BOTTLE, DROPPER (43742-2239-1)Marketed from Nov 18, 2024

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): Bact Combination
Generic name (nonproprietary): adenosinum triphosphoricum dinatrum, cinnamic acid, colibacillinum cum natrum muriaticum, streptococcus bovis dna, dysentery bacillus, echinacea (angustifolia), enterococcus faecalis, helicobacter pylori, helicobacter pylori dna, legionella pneumophila, listeria monocytogenes, malicum acidum, mycoplasma pneumoniae, natrum oxalaceticum, oroticum acidum, petroselinum sativum, pneumococcinum, proteus (mirabilis), proteus (morgani), proteus (vulgaris), pseudomonas aeruginosa, riboflavinum,
Active ingredients: Adenosine triphosphate disodium — 6 [hp_X]/mLCinnamic acid — 6 [hp_X]/mLEscherichia coli — 15 [hp_X]/mLHerring sperm DNA — 15 [hp_X]/mLShigella dysenteriae — 15 [hp_C]/mLEchinacea angustifolia whole — 15 [hp_X]/mLEnterococcus faecalis — 13 [hp_C]/mLHelicobacter pylori — 15 [hp_X]/mLHelicobacter pylori DNA — 15 [hp_X]/mLLegionella pneumophila — 14 [hp_C]/mLListeria monocytogenes — 14 [hp_C]/mLMalic acid — 6 [hp_X]/mLMycoplasma pneumoniae — 15 [hp_X]/mLSodium diethyl oxalacetate — 6 [hp_X]/mLOrotic acid monohydrate — 6 [hp_X]/mLPetroselinum crispum whole — 6 [hp_X]/mLStreptococcus pneumoniae — 13 [hp_C]/mLProteus mirabilis — 24 [hp_X]/mLProteus morganii — 30 [hp_C]/mLProteus vulgaris — 15 [hp_X]/mLPseudomonas aeruginosa — 15 [hp_X]/mLRiboflavin — 6 [hp_X]/mLSalmonella enterica enterica serovar typhi — 17 [hp_X]/mLShigella sonnei — 15 [hp_C]/mLStreptococcus agalactiae — 14 [hp_C]/mLStreptococcus equinus — 32 [hp_C]/mLStreptococcus dysgalactiae — 15 [hp_C]/mLStreptococcus mutans — 13 [hp_C]/mLStreptococcus uberis — 32 [hp_C]/mLStreptococcus viridans group — 38 [hp_C]/mL
Dosage form: Liquid
Route: Oral
Labeler: Deseret Biologicals, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Nov 18, 2024
Listing expires: Dec 31, 2026
Identifiers: Product ID 43742-2239_2b6fdcbc-1a04-48e3-9d73-d3fa213da891SPL ID 2b6fdcbc-1a04-48e3-9d73-d3fa213da891SPL set ID 0c87c329-d4a8-4e5b-9439-32a762843c7aUNII 5L51B4DR1G, U14A832J8D, 514B9K0L10, 51FI676N6F, 1EP6R5562J, VB06AV5US8, 15E04LZ9CT, U09W5JOL3Z, 14ZY3JP7M6, TJR6ZFY0F0, 3O44K14A86, 817L1N4CKP, JQE470FAD0, 6CA025Y4FG, 91532S02AO, 1WZA4Y92EX, BT6U234YR2, C177VR41DV, 56X6LID5ZY, 11T9HCO30O, Y793W5V55N, TLM2976OFR, 760T5R8B3O, OO358E3009, 2B3763S671, R2P4NKP3ZK, LN0SH02Y5M, 5C7J33MJJ1, O84V4ZK4BX, NNV2379HKRUPC 0810151880747

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

N443742223901 followed by a unit qualifier and the quantity

Package 43742-2239-01. 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 18, 2024.

Indications (excerpt from the label)

USES: • For the temporary relief of symptoms including: • mucus congestion • stomach discomfort • fever • headache • cough • joint discomfort • occasional diarrhea • bladder discomfort 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)