Immune Support
- Product NDC
- 43742-1302
- 11-digit product format
- 437421302
- Labeler code
- 43742
- Product ID
- 43742-1302_0020d8e1-ee47-4b87-81d2-ed75d193cb11
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Echinacea (Angustifolia), Arnica Montana, Baptisia Tinctoria, Sanguinaria Canadensis, Aristolochia Clematitis, Eupatorium Perfoliatum, Euphorbium Officinarum, Aconitum Napellus, Argentum Nitricum, Arsenicum Album, Bryonia (Alba), Gelsemium Sempervirens, Mercurius Corrosivus, Phosphorus, Phytolacca Decandra, Pulsatilla (Vulgaris), Rhus Tox, Sulphur, Thuja Occidentalis, Hepar Sulphuris Calcareum, Lachesis Mutus, Zincum Metallicum, Astragalus Menziesii, Influenzinum (2017-2018), Spleen (Suis), Thymus (Suis)
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Deseret Biologicals, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2018-11-07
- Marketing end
- 2024-04-16
- Substance
- ECHINACEA ANGUSTIFOLIA; ARNICA MONTANA; BAPTISIA TINCTORIA ROOT; SANGUINARIA CANADENSIS ROOT; ARISTOLOCHIA CLEMATITIS ROOT; EUPATORIUM PERFOLIATUM FLOWERING TOP; EUPHORBIA RESINIFERA RESIN; ACONITUM NAPELLUS; SILVER NITRATE; ARSENIC TRIOXIDE; BRYONIA ALBA ROOT; GELSEMIUM SEMPERVIRENS ROOT; MERCURIC CHLORIDE; PHOSPHORUS; PHYTOLACCA AMERICANA ROOT; ANEMONE PULSATILLA; TOXICODENDRON PUBESCENS LEAF; SULFUR; THUJA OCCIDENTALIS LEAFY TWIG; CALCIUM SULFIDE; LACHESIS MUTA VENOM; ZINC; ASTRAGALUS NUTTALLII LEAF; INFLUENZA A VIRUS A/SINGAPORE/GP1908/2015 IVR-180 (H1N1) ANTIGEN (FORMALDEHYDE INACTIVATED); INFLUENZA A VIRUS A/SINGAPORE/INFIMH-16-0019/2016 NIB-104 (H3N2) ANTIGEN (FORMALDEHYDE INACTIVATED); INFLUENZA B VIRUS B/MARYLAND/15/2016 ANTIGEN (FORMALDEHYDE INACTIVATED); INFLUENZA B VIRUS B/PHUKET/3073/2013 ANTIGEN (FORMALDEHYDE INACTIVATED); SUS SCROFA SPLEEN; SUS SCROFA THYMUS; VISCUM ALBUM FRUITING TOP; CORTISONE ACETATE; RANCID BEEF
- Active strength
- 1 [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; [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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43742-1302-1 | 43742130201 | 30 mL in 1 BOTTLE, DROPPER (43742-1302-1) | 30 ml | 2018-11-07 | 2024-04-16 | No | No | Current |