What is NDC 43742-2089?

43742-2089 is the product NDC for Control, Semecarpus anacardium juice 12 [hp_X]/mL + 19 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?

Control (Anacardium Orientale, Aqua Marina, Argentum Nitricum, Asarum Canadense, Blatta Orientalis, Bufo Rana, Cerebrum Suis, Clematis Erecta, Cuprum Aceticum, Hypothalamus Suis, Ignatia Amara, Kali Phosphoricum, Lachesis Mutus, Mercurius Solubilis, Natrum Sulphuricum, Placenta Totalis Suis, Rhus Tox, Thuja Occidentalis, Thymolum, Valeriana Officinalis).

What is the active ingredient?

Semecarpus anacardium juice, Sodium chloride, Silver nitrate, Asarum canadense root, Blatta orientalis, Bufo bufo cutaneous gland, Sus scrofa cerebrum, Clematis recta flowering top, Cupric acetate, Sus scrofa hypothalamus, Strychnos ignatii seed, Dibasic potassium phosphate, Lachesis muta venom, Mercurius solubilis, Sodium sulfate, Sus scrofa placenta, Toxicodendron pubescens leaf, Thuja occidentalis leafy twig, Thymol, Valerian.

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 Control?

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.

Control NDC 43742-2089 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-2089Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-2089Add 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
43742-2089-1	4374220890143742208901	30 mL in 1 BOTTLE, DROPPER (43742-2089-1)Marketed from Aug 23, 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): Control
Generic name (nonproprietary): anacardium orientale, aqua marina, argentum nitricum, asarum canadense, blatta orientalis, bufo rana, cerebrum suis, clematis erecta, cuprum aceticum, hypothalamus suis, ignatia amara, kali phosphoricum, lachesis mutus, mercurius solubilis, natrum sulphuricum, placenta totalis suis, rhus tox, thuja occidentalis, thymolum, valeriana officinalis
Active ingredients: Semecarpus anacardium juice — 12 [hp_X]/mLSodium chloride — 6 [hp_X]/mLSilver nitrate — 6 [hp_X]/mLAsarum canadense root — 12 [hp_X]/mLBlatta orientalis — 12 [hp_X]/mLBufo bufo cutaneous gland — 12 [hp_X]/mLSus scrofa cerebrum — 6 [hp_X]/mLClematis recta flowering top — 6 [hp_X]/mLCupric acetate — 6 [hp_X]/mLSus scrofa hypothalamus — 8 [hp_X]/mLStrychnos ignatii seed — 12 [hp_X]/mLDibasic potassium phosphate — 6 [hp_X]/mLLachesis muta venom — 12 [hp_X]/mLMercurius solubilis — 12 [hp_X]/mLSodium sulfate — 6 [hp_X]/mLSus scrofa placenta — 8 [hp_X]/mLToxicodendron pubescens leaf — 12 [hp_X]/mLThuja occidentalis leafy twig — 12 [hp_X]/mLThymol — 12 [hp_X]/mLValerian — 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: Aug 23, 2023
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Insect Proteins (Chemical structure)
Identifiers: Product ID 43742-2089_247ea62d-1b27-4c62-9b60-eefdc4e06723SPL ID 247ea62d-1b27-4c62-9b60-eefdc4e06723SPL set ID 9daec04d-44fb-4d0f-8e21-1109f515eb5dUNII Y0F0BU8RDU, 451W47IQ8X, 95IT3W8JZE, E2O4O7TQYK, 535787266D, Q59QU6N72Q, 4GB5DQR532, 396421SP9F, 39M11XPH03, N6R0856Z79, 1NM3M2487K, CI71S98N1Z, VSW71SS07I, 324Y4038G2, 0YPR65R21J, C8CV8867O8, 6IO182RP7A, 1NT28V9397, 3J50XA376E, JWF5YAW3QWUPC 0810151884196
Pharmacologic class: Non-Standardized Insect 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

N443742208901 followed by a unit qualifier and the quantity

Package 43742-2089-01. 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 25, 2024.

Indications (excerpt from the label)

USES: • For the temporary relief of symptoms including: • lack of self control • anger • brain support • control of emotions • rapid thoughts • obsessive thoughts • sadness • fear 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 43742-2089

What is NDC 43742-2089?: 43742-2089 is the product NDC for Control, Semecarpus anacardium juice 12 [hp_X]/mL + 19 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?: Control (Anacardium Orientale, Aqua Marina, Argentum Nitricum, Asarum Canadense, Blatta Orientalis, Bufo Rana, Cerebrum Suis, Clematis Erecta, Cuprum Aceticum, Hypothalamus Suis, Ignatia Amara, Kali Phosphoricum, Lachesis Mutus, Mercurius Solubilis, Natrum Sulphuricum, Placenta Totalis Suis, Rhus Tox, Thuja Occidentalis, Thymolum, Valeriana Officinalis).
What is the active ingredient?: Semecarpus anacardium juice, Sodium chloride, Silver nitrate, Asarum canadense root, Blatta orientalis, Bufo bufo cutaneous gland, Sus scrofa cerebrum, Clematis recta flowering top, Cupric acetate, Sus scrofa hypothalamus, Strychnos ignatii seed, Dibasic potassium phosphate, Lachesis muta venom, Mercurius solubilis, Sodium sulfate, Sus scrofa placenta, Toxicodendron pubescens leaf, Thuja occidentalis leafy twig, Thymol, Valerian.
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 Control?: 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.