What is NDC 43742-2532?

43742-2532 is the product NDC for PARV Plus, Antimony trisulfide 12 [hp_X]/mL + 8 more ingredients liquid, listed with the FDA by Deseret Biologicals, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

PARV Plus (Antimonium Crudum, Apis Mellifica, Chamomilla, Echinacea (Angustifolia), Ferrum Phosphoricum, Pulsatilla (Pratensis), Rhus Tox, Sulphur, Urtica Urens).

What is the active ingredient?

Antimony trisulfide, Apis mellifera, Matricaria chamomilla whole, Echinacea angustifolia whole, Ferrosoferric phosphate, Pulsatilla pratensis whole, Toxicodendron pubescens leaf, Sulfur, Urtica urens whole.

Deseret Biologicals, Inc., NDC labeler code 43742. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for PARV Plus?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

PARV Plus NDC 43742-2532 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-2532Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-2532Add 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
43742-2532-1	4374225320143742253201	30 mL in 1 BOTTLE, DROPPER (43742-2532-1)Marketed from Jan 2, 2026

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): PARV Plus
Generic name (nonproprietary): antimonium crudum, apis mellifica, chamomilla, echinacea (angustifolia), ferrum phosphoricum, pulsatilla (pratensis), rhus tox, sulphur, urtica urens
Active ingredients: Antimony trisulfide — 12 [hp_X]/mLApis mellifera — 12 [hp_X]/mLMatricaria chamomilla whole — 6 [hp_X]/mLEchinacea angustifolia whole — 6 [hp_X]/mLFerrosoferric phosphate — 12 [hp_X]/mLPulsatilla pratensis whole — 12 [hp_X]/mLToxicodendron pubescens leaf — 12 [hp_X]/mLSulfur — 12 [hp_X]/mLUrtica urens whole — 6 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Deseret Biologicals, Inc.NDC labeler code 43742
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jan 2, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Allergens (Chemical structure)Bee Venoms (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)
Identifiers: Product ID 43742-2532_81d00235-5b69-4a5b-9f35-7af9fc8b6dc7SPL ID 81d00235-5b69-4a5b-9f35-7af9fc8b6dc7SPL set ID 187113bf-fcec-4942-8343-dc200bd3e5e9UNII F79059A38U, 7S82P3R43Z, G0R4UBI2ZZ, VB06AV5US8, 91GQH8I5F7, 8E272251DI, 6IO182RP7A, 70FD1KFU70, IHN2NQ5OF9UPC 0810151885056
Pharmacologic class: Standardized Insect Venom Allergenic Extract

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

N443742253201 followed by a unit qualifier and the quantity

Package 43742-2532-01. 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 Jan 2, 2026.

Indications (excerpt from the label)

USES: • For the temporary relief of symptoms including: • immune support • fever • fatigue • sore throat • cough • runny nose • rash • joint pain • muscle aches 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)

About NDC 43742-2532

What is NDC 43742-2532?: 43742-2532 is the product NDC for PARV Plus, Antimony trisulfide 12 [hp_X]/mL + 8 more ingredients liquid, listed with the FDA by Deseret Biologicals, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: PARV Plus (Antimonium Crudum, Apis Mellifica, Chamomilla, Echinacea (Angustifolia), Ferrum Phosphoricum, Pulsatilla (Pratensis), Rhus Tox, Sulphur, Urtica Urens).
What is the active ingredient?: Antimony trisulfide, Apis mellifera, Matricaria chamomilla whole, Echinacea angustifolia whole, Ferrosoferric phosphate, Pulsatilla pratensis whole, Toxicodendron pubescens leaf, Sulfur, Urtica urens whole.
Who is the labeler?: Deseret Biologicals, Inc., NDC labeler code 43742. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for PARV Plus?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.