NDC 43742-1759 – Cand Plus

Goldenseal 5 [hp_X]/mL; Berberis Vulgaris Root Bark 6 [hp_X]/mL; Sodium Borate 6 [hp_X]/mL; Sucrose 6 [hp_X]/mL; Caffeine 6 [hp_X]/mL; Gallic Acid Monohydrate… · Liquid · Oral

Human Otc Drug

Product NDC43742-1759

Product details

Brand name
Cand Plus
Generic name
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
Labeler
Deseret Biologicals, Inc.
Dosage form
Liquid
Route
Oral
Marketing category
UNAPPROVED HOMEOPATHIC
Marketed since
September 22, 2020
Listing expires
December 31, 2026
Pharmacologic class
Central Nervous System Stimulant; Methylxanthine; Non-Standardized Food Allergenic Extract; Non-Standardized Food Allergenic Extract; Non-Standardized Fungal Allergenic Extract; Non-Standardized Fungal Allergenic Extract; Non-Standardized Fungal Allergenic Extract

Active ingredients

Uses, dosage, side effects and warnings for Cand Plus →

Package NDC codes (1)

Package NDCDescriptionSince
43742-1759-130 mL in 1 BOTTLE, DROPPER (43742-1759-1)Sep 22, 2020