What is NDC 43742-2177?

43742-2177 is the product NDC for BP Reg, Epinephrine 8 [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?

BP Reg (Adrenalinum, Allium Sativum, Alpha-Lipoicum Acidum, Arteria Suis, Aurum Metallicum, Cactus Grandiflorus, Cholesterinum, Cortisone Aceticum, Coumarinum, Formalinum, Glonoinum, Kali Chloricum, Lachesis Mutus, Proteus (Vulgaris), Rauwolfia Serpentina, Strontium Carbonicum, Sulphur, Thyroidinum (Suis), Vena Suis, Veratrum Album).

What is the active ingredient?

Epinephrine, Garlic, Alpha lipoic acid, Sus scrofa artery, Gold, Selenicereus grandiflorus stem, Cholesterol, Cortisone acetate, Coumarin, Formaldehyde solution, Nitroglycerin, Potassium chlorate, Lachesis muta venom, Proteus vulgaris, Rauwolfia serpentina, Strontium carbonate, Sulfur, Thyroid, Sus scrofa vein, Veratrum album root.

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 BP Reg?

1 other product NDC are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

BP Reg NDC 43742-2177 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-2177Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-2177Add 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
43742-2177-1	4374221770143742217701	30 mL in 1 BOTTLE, DROPPER (43742-2177-1)Marketed from May 9, 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): BP Reg
Generic name (nonproprietary): adrenalinum, allium sativum, alpha-lipoicum acidum, arteria suis, aurum metallicum, cactus grandiflorus, cholesterinum, cortisone aceticum, coumarinum, formalinum, glonoinum, kali chloricum, lachesis mutus, proteus (vulgaris), rauwolfia serpentina, strontium carbonicum, sulphur, thyroidinum (suis), vena suis, veratrum album
Active ingredients: Epinephrine — 8 [hp_X]/mLGarlic — 6 [hp_X]/mLAlpha lipoic acid — 12 [hp_X]/mLSus scrofa artery — 8 [hp_X]/mLGold — 12 [hp_X]/mLSelenicereus grandiflorus stem — 12 [hp_X]/mLCholesterol — 12 [hp_X]/mLCortisone acetate — 8 [hp_X]/mLCoumarin — 12 [hp_X]/mLFormaldehyde solution — 9 [hp_X]/mLNitroglycerin — 12 [hp_X]/mLPotassium chlorate — 9 [hp_X]/mLLachesis muta venom — 12 [hp_X]/mLProteus vulgaris — 16 [hp_X]/mLRauwolfia serpentina — 12 [hp_X]/mLStrontium carbonate — 12 [hp_X]/mLSulfur — 12 [hp_X]/mLThyroid — 8 [hp_X]/mLSus scrofa vein — 8 [hp_X]/mLVeratrum album root — 12 [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: May 9, 2024
Listing expires: Dec 31, 2026
Other FDA classes: Adrenergic alpha-Agonists (Mechanism)Adrenergic beta-Agonists (Mechanism)Allergens (Chemical structure)Allergens (Chemical structure)Catecholamines (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Corticosteroid Hormone Receptor Agonists (Mechanism)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Nitrates (Chemical structure)Osmotic Activity (Mechanism)Plant Proteins (Chemical structure)Potassium Compounds (Chemical structure)Vasodilation (Physiologic effect)
Identifiers: Product ID 43742-2177_fc50a508-522c-45e0-8ef7-0d6c684e88ffSPL ID fc50a508-522c-45e0-8ef7-0d6c684e88ffSPL set ID 540c1149-b6d4-4926-87e8-73a920f87b4aUNII YKH834O4BH, V1V998DC17, 73Y7P0K73Y, 63O327782Q, 79Y1949PYO, 7114SV0MYK, 97C5T2UQ7J, 883WKN7W8X, A4VZ22K1WT, T0H3L6C7I5, G59M7S0WS3, H35KS68EE7, VSW71SS07I, 11T9HCO30O, H192N84N1G, 41YPU4MMCA, 70FD1KFU70, 6RV024OAUQ, 2510RH3I89, QNS6W5US1ZUPC 0810151883656
Pharmacologic class: Catecholamine; Corticosteroid; Nitrate Vasodilator; Non-Standardized Food Allergenic Extract; Osmotic Laxative; Potassium Salt; Standardized Chemical Allergen; alpha-Adrenergic Agonist; beta-Adrenergic Agonist

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

N443742217701 followed by a unit qualifier and the quantity

Package 43742-2177-01. 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: • headache • fatigue • confusion • intimacy issues 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 43742-2177

What is NDC 43742-2177?: 43742-2177 is the product NDC for BP Reg, Epinephrine 8 [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?: BP Reg (Adrenalinum, Allium Sativum, Alpha-Lipoicum Acidum, Arteria Suis, Aurum Metallicum, Cactus Grandiflorus, Cholesterinum, Cortisone Aceticum, Coumarinum, Formalinum, Glonoinum, Kali Chloricum, Lachesis Mutus, Proteus (Vulgaris), Rauwolfia Serpentina, Strontium Carbonicum, Sulphur, Thyroidinum (Suis), Vena Suis, Veratrum Album).
What is the active ingredient?: Epinephrine, Garlic, Alpha lipoic acid, Sus scrofa artery, Gold, Selenicereus grandiflorus stem, Cholesterol, Cortisone acetate, Coumarin, Formaldehyde solution, Nitroglycerin, Potassium chlorate, Lachesis muta venom, Proteus vulgaris, Rauwolfia serpentina, Strontium carbonate, Sulfur, Thyroid, Sus scrofa vein, Veratrum album root.
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 BP Reg?: 1 other product NDC are listed under this name. See all BP Reg NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other BP Reg NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
BP Regallium sativum, adrenalinum, arteria suis, cortisone aceticum, thyroidinum (suis), vena suis, formalinum, kali chloricum, alpha-lipoicum acidum, aurum metallicum, cactus grandiflorus, cholesterinum, coumarinum, ephedra vulgaris, glonoinum, lachesis mutus, rauwolfia serpentina, strontium carbonicum, sulphur, veratrum album, proteus (vulgaris)	Garlic 6 [hp_X]/mL + 20 more ingredients	LiquidOral	Deseret Biologicals, Inc.	43742-1414	43742-1414-01