Home NDC 43742-2195 Gum Therapy
Product NDC 43742-2195
11-digit product format 437422195
Labeler code 43742
Product ID 43742-2195_241225bd-9b79-47fb-9549-45581ea327c3
Type HUMAN OTC DRUG
Nonproprietary name Aconitum Napellus, Arnica Montana, Bismuthum Subnitricum, Borax, Calcarea Fluorica, Calendula Officinalis, Cistus Canadensis, Hepar Sulphuris Calcareum, Kali Phosphoricum, Kreosotum, Mercurius Vivus, Myrrha, Natrum Muriaticum, Sepia
Dosage form LIQUID
Route ORAL
Labeler Deseret Biologicals
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2024-08-28
Substance ACONITUM NAPELLUS WHOLE; ARNICA MONTANA WHOLE; BISMUTH SUBNITRATE; SODIUM BORATE; CALCIUM FLUORIDE; CALENDULA OFFICINALIS FLOWERING TOP; HELIANTHEMUM CANADENSE; CALCIUM SULFIDE; DIBASIC POTASSIUM PHOSPHATE; WOOD CREOSOTE; MERCURY; MYRRH; SODIUM CHLORIDE; SEPIA OFFICINALIS JUICE
Active strength 12; 3; 12; 6; 8; 1; 12; 12; 3; 6; 12; 6; 3; 12 [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
Pharmacologic classes Bismuth [CS], Bismuth [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Gum Therapy
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ACONITUM NAPELLUS WHOLE 12 [hp_X]/mL ARNICA MONTANA WHOLE 3 [hp_X]/mL BISMUTH SUBNITRATE 12 [hp_X]/mL SODIUM BORATE 6 [hp_X]/mL CALCIUM FLUORIDE 8 [hp_X]/mL CALENDULA OFFICINALIS FLOWERING TOP 1 [hp_X]/mL HELIANTHEMUM CANADENSE 12 [hp_X]/mL CALCIUM SULFIDE 12 [hp_X]/mL DIBASIC POTASSIUM PHOSPHATE 3 [hp_X]/mL WOOD CREOSOTE 6 [hp_X]/mL MERCURY 12 [hp_X]/mL MYRRH 6 [hp_X]/mL SODIUM CHLORIDE 3 [hp_X]/mL SEPIA OFFICINALIS JUICE 12 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 14 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 43742-2195-1 Gum Therapy 30 mL in 1 BOTTLE, DROPPER LIQUID 30 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 43742-2195 GUM THERAPY (ACONITUM NAPELLUS, ARNICA MONTANA, BISMUTHUM SUBNITRICUM, BORAX, CALCAREA FLUORICA, CALENDULA OFFICINALIS, CISTUS CANADENSIS, HEPAR SULPHURIS CALCAREUM, KALI PHOSPHORICUM, KREOSOTUM, MERCURIUS VIVUS, MYRRHA, NATRUM MURIATICUM, SEPIA) LIQUID [DESERET BIOLOGICALS] 2 Current NDC, 1 package rows 20240830_ceb5203b-b4c8-4c7b-8e18-ccbff5034fc1.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Gum Therapy ACONITUM NAPELLUS, ARNICA MONTANA, BISMUTHUM SUBNITRICUM, BORAX, CALCAREA FLUORICA, CALENDULA OFFICINALIS, CISTUS CANADENSIS, HEPAR SULPHURIS CALCAREUM, KALI PHOSPHORICUM, KREOSOTUM, MERCURIUS VIVUS, MYRRHA, NATRUM MURIATICUM, SEPIA Deseret Biologicals ceb5203b-b4c8-4c7b-8e18-ccbff5034fc1 2024-08-29 Warnings Exact identifier ndc (product): 43742-2195
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 43742-2195-1 43742219501 30 mL in 1 BOTTLE, DROPPER (43742-2195-1) 30 ml 2024-08-28 No No Current