Home NDC 43742-2088 Gum Therapy
Product NDC 43742-2088
11-digit product format 437422088
Labeler code 43742
Product ID 43742-2088_65c157e4-e2fb-43c8-a0e3-810a46dbe515
Type HUMAN OTC DRUG
Nonproprietary name Calendula Officinalis, Kali Phosphoricum, Natrum Muriaticum, Arnica Montana, Borax, Cistus Canadensis, Kreosotum, Myrrha, Calcarea Fluorica, Aconitum Napellus, Bismuthum Subnitricum, Sepia, Hepar Sulphuris Calcareum, Mercurius Vivus
Dosage form LIQUID
Route ORAL
Labeler Deseret Biologicals
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2023-07-19
Marketing end 2028-08-10
Substance CALENDULA OFFICINALIS FLOWERING TOP; DIBASIC POTASSIUM PHOSPHATE; SODIUM CHLORIDE; ARNICA MONTANA WHOLE; SODIUM BORATE; HELIANTHEMUM CANADENSE; WOOD CREOSOTE; MYRRH; CALCIUM FLUORIDE; ACONITUM NAPELLUS WHOLE; BISMUTH SUBNITRATE; SEPIA OFFICINALIS JUICE; CALCIUM SULFIDE; MERCURY
Active strength 1; 3; 3; 3; 6; 6; 6; 6; 8; 12; 12; 12; 12; 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
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 Active Ingredients# Ingredient, Strength table Ingredient Strength CALENDULA OFFICINALIS FLOWERING TOP 1 [hp_X]/mL DIBASIC POTASSIUM PHOSPHATE 3 [hp_X]/mL SODIUM CHLORIDE 3 [hp_X]/mL ARNICA MONTANA WHOLE 3 [hp_X]/mL SODIUM BORATE 6 [hp_X]/mL HELIANTHEMUM CANADENSE 6 [hp_X]/mL WOOD CREOSOTE 6 [hp_X]/mL MYRRH 6 [hp_X]/mL CALCIUM FLUORIDE 8 [hp_X]/mL ACONITUM NAPELLUS WHOLE 12 [hp_X]/mL BISMUTH SUBNITRATE 12 [hp_X]/mL SEPIA OFFICINALIS JUICE 12 [hp_X]/mL CALCIUM SULFIDE 12 [hp_X]/mL MERCURY 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 43742-2088-1 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 43742-2088 GUM THERAPY (CALENDULA OFFICINALIS, KALI PHOSPHORICUM, NATRUM MURIATICUM, ARNICA MONTANA, BORAX, CISTUS CANADENSIS, KREOSOTUM, MYRRHA, CALCAREA FLUORICA, ACONITUM NAPELLUS, BISMUTHUM SUBNITRICUM, SEPIA, HEPAR SULPHURIS CALCAREUM, MERCURIUS VIVUS) LIQUID [DESERET BIOLOGICALS] 2 Current NDC, 1 package rows 20240830_5c741edc-f3ce-4e43-bb3e-fb7316621406.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 CALENDULA OFFICINALIS, KALI PHOSPHORICUM, NATRUM MURIATICUM, ARNICA MONTANA, BORAX, CISTUS CANADENSIS, KREOSOTUM, MYRRHA, CALCAREA FLUORICA, ACONITUM NAPELLUS, BISMUTHUM SUBNITRICUM, SEPIA, HEPAR SULPHURIS CALCAREUM, MERCURIUS VIVUS Deseret Biologicals 5c741edc-f3ce-4e43-bb3e-fb7316621406 2024-08-28 Warnings Exact identifier ndc (product): 43742-2088
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 43742-2088-1 43742208801 30 mL in 1 BOTTLE, DROPPER (43742-2088-1) 30 ml 2023-07-19 2028-08-10 No No Historical