What is NDC 43742-1414?

43742-1414 is the product NDC for BP Reg, Garlic 6 [hp_X]/mL + 20 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 (Allium 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)).

What is the active ingredient?

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

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 43742-1414 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-1414Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-1414Add 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
43742-1414-1	4374214140143742141401	30 mL in 1 BOTTLE, DROPPER (43742-1414-1)Marketed from Dec 6, 2018

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): allium 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)
Active ingredients: Garlic — 6 [hp_X]/mLEpinephrine — 8 [hp_X]/mLSus scrofa artery — 8 [hp_X]/mLCortisone acetate — 8 [hp_X]/mLThyroid — 8 [hp_X]/mLSus scrofa vein — 8 [hp_X]/mLFormaldehyde — 9 [hp_X]/mLPotassium chlorate — 9 [hp_X]/mLThioctic acid — 12 [hp_X]/mLGold — 12 [hp_X]/mLSelenicereus grandiflorus stem — 12 [hp_X]/mLCholesterol — 12 [hp_X]/mLCoumarin — 12 [hp_X]/mLEphedra distachya flowering twig — 12 [hp_X]/mLNitroglycerin — 12 [hp_X]/mLLachesis muta venom — 12 [hp_X]/mLRauwolfia serpentina — 12 [hp_X]/mLStrontium carbonate — 12 [hp_X]/mLSulfur — 12 [hp_X]/mLVeratrum album root — 12 [hp_X]/mLProteus vulgaris — 16 [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: Dec 6, 2018
Marketing end: Feb 21, 2029
Other FDA classes: Adrenergic alpha-Agonists (Mechanism)Adrenergic beta-Agonists (Mechanism)Allergens (Chemical structure)Allergens (Chemical structure)Allergens (Chemical structure)Catecholamines (Chemical structure)Cell-mediated Immunity (Physiologic effect)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 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 43742-1414_44080616-63f6-4943-a9ef-b8a0e4a07a82SPL ID 44080616-63f6-4943-a9ef-b8a0e4a07a82SPL set ID f99833d8-d637-4c63-afe8-25eb2f05de6aUNII V1V998DC17, YKH834O4BH, 63O327782Q, 883WKN7W8X, 6RV024OAUQ, 2510RH3I89, 1HG84L3525, H35KS68EE7, 73Y7P0K73Y, 79Y1949PYO, 7114SV0MYK, 97C5T2UQ7J, A4VZ22K1WT, R55VQ87DP3, G59M7S0WS3, VSW71SS07I, H192N84N1G, 41YPU4MMCA, 70FD1KFU70, QNS6W5US1Z, 11T9HCO30OUPC 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

N443742141401 followed by a unit qualifier and the quantity

Package 43742-1414-01. 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 8, 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 43742-1414

What is NDC 43742-1414?: 43742-1414 is the product NDC for BP Reg, Garlic 6 [hp_X]/mL + 20 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 (Allium 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)).
What is the active ingredient?: Garlic, Epinephrine, Sus scrofa artery, Cortisone acetate, Thyroid, Sus scrofa vein, Formaldehyde, Potassium chlorate, Thioctic acid, Gold, Selenicereus grandiflorus stem, Cholesterol, Coumarin, Ephedra distachya flowering twig, Nitroglycerin, Lachesis muta venom, Rauwolfia serpentina, Strontium carbonate, Sulfur, Veratrum album root, Proteus vulgaris.
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 Regadrenalinum, 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	Epinephrine 8 [hp_X]/mL + 19 more ingredients	LiquidOral	Deseret Biologicals, Inc.	43742-2177	43742-2177-01