Oral Health

Product NDC

43742-1511

11-digit product format

437421511

Labeler code

43742

Product ID

43742-1511_aa8abc78-8cad-43d1-919e-714b5b5580f1

Type

HUMAN OTC DRUG

Nonproprietary name

Borax, Bryonia (Alba), Echinacea Purpurea, Juglans Cinerea, Kali Muriaticum, Magnesia Muriatica, Muriaticum Acidum, Discus Intervertebralis Suis, Oral Mucosa (Suis), Antimonium Crudum, Arsenicum Album, Bismuthum Subnitricum, Chamomilla, Cinchona Officinalis, Nux Moschata, Sambucus Nigra, Sepia, Mercurius Solubilis, Calcarea Phosphorica, Ignatia Amara, Oxygenium, Candida Albicans

Dosage form

LIQUID

Route

ORAL

Labeler

Deseret Biologicals, Inc.

Marketing category

UNAPPROVED HOMEOPATHIC

Marketing start

2019-08-20

Marketing end

2024-10-22

Substance

SODIUM BORATE; BRYONIA ALBA ROOT; ECHINACEA PURPUREA; JUGLANS CINEREA BRANCH BARK/ROOT BARK; POTASSIUM CHLORIDE; MAGNESIUM CHLORIDE; HYDROCHLORIC ACID; SUS SCROFA INTERVERTEBRAL DISC; SUS SCROFA ORAL MUCOSA; ANTIMONY TRISULFIDE; ARSENIC TRIOXIDE; BISMUTH SUBNITRATE; MATRICARIA CHAMOMILLA; CINCHONA OFFICINALIS BARK; NUTMEG; SAMBUCUS NIGRA FLOWERING TOP; SEPIA OFFICINALIS JUICE; MERCURIUS SOLUBILIS; TRIBASIC CALCIUM PHOSPHATE; STRYCHNOS IGNATII SEED; OXYGEN; CANDIDA ALBICANS

Active strength

6 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record