Gum Therapy
- Product NDC
- 43742-1244
- 11-digit product format
- 437421244
- Labeler code
- 43742
- Product ID
- 43742-1244_1fdebd1a-db6f-4b86-aa09-49fe5ade6402
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Calendula Officinalis, Eugenia Caryophyllata, Plantago Major, Arnica Montana, Phytolacca Decandra, Phosphorus, Peptostreptococcus Anaerobius, Carbo Vegetabilis, Hepar Sulphuris Calcareum, Lachesis Mutus, Mercurius Solubilis
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Deseret Biologicals
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2018-07-10
- Marketing end
- 2024-08-01
- Substance
- ACTIVATED CHARCOAL; ARNICA MONTANA; CALCIUM SULFIDE; CALENDULA OFFICINALIS FLOWERING TOP; CLOVE; LACHESIS MUTA VENOM; MERCURIUS SOLUBILIS; PEPTOSTREPTOCOCCUS ANAEROBIUS; PHOSPHORUS; PHYTOLACCA AMERICANA ROOT; PLANTAGO MAJOR
- Active strength
- 30 [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
- Pharmacologic classes
- Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Food Additives [CS], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43742-1244-1 | 43742124401 | 30 mL in 1 BOTTLE, DROPPER (43742-1244-1) | 30 ml | 2018-07-10 | 2024-08-01 | No | No | Current |