NDC 43406-0672 – Candida HP

Baptisia Tinctoria Root 4 [hp_X]/mL; Echinacea Purpurea 4 [hp_X]/mL; Glycyrrhiza Glabra 4 [hp_X]/mL; Astragalus Nuttallii Leaf 6 [hp_X]/mL; Sodium Borate 30… · Liquid · Oral

Human Otc Drug

Product NDC43406-0672

Product details

Brand name
Candida HP
Generic name
Baptisia Tinctoria Root, Echinacea Purpurea, Glycyrrhiza Glabra, Astragalus Nuttallii Leaf, Candida Albicans, Sodium Borate, Oyster Shell Calcium Carbonate, Crude, Wood Creosote, Lycopodium Clavatum Spore, Strychnos Nux-Vomica Seed, Phosphoric Acid, Anemone Pulsatilla, Sepia Officinalis Juice, Thuja Occidentalis Leafy Twig, Sodium Phosphate, Dibasic, Heptahydrate, Nitric Acid
Labeler
Natural Creations, Inc.
Dosage form
Liquid
Route
Oral
Marketing category
UNAPPROVED HOMEOPATHIC
Marketed since
January 1, 2018
Listing expires
December 31, 2026
Pharmacologic class
Non-Standardized Food Allergenic Extract; Non-Standardized Fungal Allergenic Extract; Non-Standardized Plant Allergenic Extract; Non-Standardized Plant Allergenic Extract

Active ingredients

Uses, dosage, side effects and warnings for Candida HP →

Package NDC codes (1)

Package NDCDescriptionSince
43406-0672-130 mL in 1 BOTTLE, DROPPER (43406-0672-1)Jan 1, 2018