What is NDC 43742-1759?

43742-1759 is the product NDC for Cand Plus, Goldenseal 5 [hp_X]/mL + 17 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?

Cand Plus (Hydrastis Canadensis, Berberis Vulgaris, Borax, Saccharum Officinale, Caffeinum, Gallicum Acidum, Indolum, Allium Sativum, Echinacea (Angustifolia), Asafoetida, Acetaldehyde, Folliculinum, Lycopodium Clavatum, Phytolacca Decandra, Pulsatilla (Pratensis), Sepia, Ustilago Maidis, Torula Cerevisiae).

What is the active ingredient?

Goldenseal, Berberis vulgaris root bark, Sodium borate, Sucrose, Caffeine, Gallic acid monohydrate, Indole, Garlic, Echinacea angustifolia whole, Ferula assa-foetida resin, Acetaldehyde, Estrone, Lycopodium clavatum spore, Phytolacca americana root, Pulsatilla pratensis whole, Sepia officinalis juice, Ustilago maydis, Saccharomyces cerevisiae.

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 Cand 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.

Cand Plus NDC 43742-1759 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-1759Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-1759Add 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
43742-1759-1	4374217590143742175901	30 mL in 1 BOTTLE, DROPPER (43742-1759-1)Marketed from Sep 22, 2020

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): Cand Plus
Generic name (nonproprietary): hydrastis canadensis, berberis vulgaris, borax, saccharum officinale, caffeinum, gallicum acidum, indolum, allium sativum, echinacea (angustifolia), asafoetida, acetaldehyde, folliculinum, lycopodium clavatum, phytolacca decandra, pulsatilla (pratensis), sepia, ustilago maidis, torula cerevisiae
Active ingredients: Goldenseal — 5 [hp_X]/mLBerberis vulgaris root bark — 6 [hp_X]/mLSodium borate — 6 [hp_X]/mLSucrose — 6 [hp_X]/mLCaffeine — 6 [hp_X]/mLGallic acid monohydrate — 6 [hp_X]/mLIndole — 6 [hp_X]/mLGarlic — 8 [hp_X]/mLEchinacea angustifolia whole — 8 [hp_X]/mLFerula assa-foetida resin — 8 [hp_X]/mLAcetaldehyde — 8 [hp_X]/mLEstrone — 12 [hp_X]/mLLycopodium clavatum spore — 12 [hp_X]/mLPhytolacca americana root — 12 [hp_X]/mLPulsatilla pratensis whole — 12 [hp_X]/mLSepia officinalis juice — 12 [hp_X]/mLUstilago maydis — 12 [hp_X]/mLSaccharomyces cerevisiae — 60 [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: Sep 22, 2020
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Allergens (Chemical structure)Allergens (Chemical structure)Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Central Nervous System Stimulation (Physiologic effect)Dietary Proteins (Chemical structure)Dietary Proteins (Chemical structure)Fungal Proteins (Chemical structure)Fungal Proteins (Chemical structure)Fungal Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Xanthines (Chemical structure)
Identifiers: Product ID 43742-1759_8685fe17-ad92-4ce8-9894-2b457f1c1cb0SPL ID 8685fe17-ad92-4ce8-9894-2b457f1c1cb0SPL set ID 1f8ab864-27c2-4457-8ad7-5d65f9983e2cUNII ZW3Z11D0JV, 1TH8Q20J0U, 91MBZ8H3QO, C151H8M554, 3G6A5W338E, 48339473OT, 8724FJW4M5, V1V998DC17, VB06AV5US8, W9FZA51AS1, GO1N1ZPR3B, 2DI9HA706A, C88X29Y479, 11E6VI8VEG, 8E272251DI, QDL83WN8C2, 4K7Z7K7SWG, 978D8U419HUPC 0810151880334
Pharmacologic class: Central Nervous System Stimulant; Methylxanthine; Non-Standardized Food Allergenic Extract; Non-Standardized Fungal 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

N443742175901 followed by a unit qualifier and the quantity

Package 43742-1759-01. 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 6, 2024.

Indications (excerpt from the label)

USES: • For the temporary relief of symptoms including: • mucous congestion • nausea • drowsiness • lethargy • confusion • vaginal discharge • sensitivity to foods 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 43742-1759

What is NDC 43742-1759?: 43742-1759 is the product NDC for Cand Plus, Goldenseal 5 [hp_X]/mL + 17 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?: Cand Plus (Hydrastis Canadensis, Berberis Vulgaris, Borax, Saccharum Officinale, Caffeinum, Gallicum Acidum, Indolum, Allium Sativum, Echinacea (Angustifolia), Asafoetida, Acetaldehyde, Folliculinum, Lycopodium Clavatum, Phytolacca Decandra, Pulsatilla (Pratensis), Sepia, Ustilago Maidis, Torula Cerevisiae).
What is the active ingredient?: Goldenseal, Berberis vulgaris root bark, Sodium borate, Sucrose, Caffeine, Gallic acid monohydrate, Indole, Garlic, Echinacea angustifolia whole, Ferula assa-foetida resin, Acetaldehyde, Estrone, Lycopodium clavatum spore, Phytolacca americana root, Pulsatilla pratensis whole, Sepia officinalis juice, Ustilago maydis, Saccharomyces cerevisiae.
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 Cand 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.