What is NDC 43742-1258?

43742-1258 is the product NDC for Bio Mood Phase, Cortisone acetate 8 [hp_C]/mL + 9 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?

Bio Mood Phase (Cortisone Aceticum, Adrenalinum, Chininum Arsenicosum, Helonias Dioica, Hypericum Perforatum, Kali Phosphoricum, Nux Vomica, Selenium Metallicum, Aurum Metallicum, Bacillus 7 (Enterobacter Cloacae)).

What is the active ingredient?

Cortisone acetate, Epinephrine, Quinine arsenate, Chamaelirium luteum root, Hypericum perforatum whole, Dibasic potassium phosphate, Strychnos nux-vomica seed, Selenium, Gold, Enterobacter cloacae.

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 Bio Mood Phase?

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.

Bio Mood Phase NDC 43742-1258 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-1258Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-1258Add 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
43742-1258-1	4374212580143742125801	30 mL in 1 BOTTLE, DROPPER (43742-1258-1)Marketed from Sep 11, 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): Bio Mood Phase
Generic name (nonproprietary): cortisone aceticum, adrenalinum, chininum arsenicosum, helonias dioica, hypericum perforatum, kali phosphoricum, nux vomica, selenium metallicum, aurum metallicum, bacillus 7 (enterobacter cloacae)
Active ingredients: Cortisone acetate — 8 [hp_C]/mLEpinephrine — 8 [hp_C]/mLQuinine arsenate — 10 [hp_C]/mLChamaelirium luteum root — 10 [hp_C]/mLHypericum perforatum whole — 10 [hp_C]/mLDibasic potassium phosphate — 10 [hp_C]/mLStrychnos nux-vomica seed — 10 [hp_C]/mLSelenium — 10 [hp_C]/mLGold — 10 [hp_C]/mLEnterobacter cloacae — 30 [hp_C]/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: Sep 11, 2018
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)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 43742-1258_d75fc007-3071-4114-9cb5-4aa4686778a3SPL ID d75fc007-3071-4114-9cb5-4aa4686778a3SPL set ID 81d6e6db-94dc-4b6f-9ef7-9180ec54eebfUNII 883WKN7W8X, YKH834O4BH, 8C15XFK30P, DQV54Y5H3U, XK4IUX8MNB, CI71S98N1Z, 269XH13919, H6241UJ22B, 79Y1949PYO, 40OMQ8YEPDUPC 0810151881713
Pharmacologic class: Antimalarial; Catecholamine; Corticosteroid; Non-Standardized Plant Allergenic Extract; 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

N443742125801 followed by a unit qualifier and the quantity

Package 43742-1258-01. 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 Apr 26, 2024.

Indications (excerpt from the label)

USES: • For the temporary relief of symptoms including: • emotional distress • nervous anxiety • nervous exhaustion 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 43742-1258

What is NDC 43742-1258?: 43742-1258 is the product NDC for Bio Mood Phase, Cortisone acetate 8 [hp_C]/mL + 9 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?: Bio Mood Phase (Cortisone Aceticum, Adrenalinum, Chininum Arsenicosum, Helonias Dioica, Hypericum Perforatum, Kali Phosphoricum, Nux Vomica, Selenium Metallicum, Aurum Metallicum, Bacillus 7 (Enterobacter Cloacae)).
What is the active ingredient?: Cortisone acetate, Epinephrine, Quinine arsenate, Chamaelirium luteum root, Hypericum perforatum whole, Dibasic potassium phosphate, Strychnos nux-vomica seed, Selenium, Gold, Enterobacter cloacae.
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 Bio Mood Phase?: 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.