Natural Relief Cough and Congestion

NDC 17312-432 · TRP Company

Generic nameAntimonium tartaricum, Coccus cacti, Cuprum metallicum, Drosera rotundifolia, Echinacea angustifolia, Kali carbonicum, Mephitis mephitica, Natrum muriaticum, Rumex crispus, Zincum gluconicum

Dosage formSPRAY

RouteORAL

Active ingredient(s)ANTIMONY POTASSIUM TARTRATE, ZINC GLUCONATE, RUMEX CRISPUS ROOT, SODIUM CHLORIDE, MEPHITIS MEPHITIS ANAL GLAND FLUID, POTASSIUM CARBONATE, ECHINACEA ANGUSTIFOLIA, DROSERA ROTUNDIFOLIA, COPPER, PROTORTONIA CACTI

Strength6; 6; 6; 6; 12; 6; 6; 6; 6; 4 [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL

Pharmacologic classCopper Absorption Inhibitor [EPC], Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Copper Ion Absorption [PE], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Increased Large Intestinal Motility [PE], Inhibit Ovum Fertilization [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC]

Marketing categoryUNAPPROVED HOMEOPATHIC

Packages

17312-432-23 — 1 BOTTLE, SPRAY in 1 CARTON (17312-432-23) / 20 mL in 1 BOTTLE, SPRAY

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

17271-710 — SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE, 17271-734 — DEXTROSE MONOHYDRATE and SODIUM CHLORIDE, 17271-735 — DEXTROSE MONOHYDRATE and SODIUM CHLORIDE, 17271-771 — SODIUM CHLORIDE, 17271-800 — SODIUM CHLORIDE, 17312-018 — ANTIMONY POTASSIUM TARTRATE - PROTORTONIA CACTI - DROSERA ROTUNDIFOLIA - ECHINACEA, UNSPECIFIED - CALCIUM SULFIDE - HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED - SPONGIA OFFICINALIS SKELETON, ROASTED -, 17312-041 — ATROPA BELLADONNA - BRYONIA ALBA ROOT - BLACK COHOSH - ARABICA COFFEE BEAN - NITROGLYCERIN - IRIS VERSICOLOR ROOT - SODIUM CHLORIDE -, 17312-077 — Bryonia, Gelsemium sempervirens, Sambucus nigra, Sulphur, Zincum gluconicum, 17312-173 — Apis mellifica, Arnica montana, Calcarea phosphorica, Chamomilla,Echinacea, Hepar sulphuris calcareum, Hoitzia, Passiflora, Valeriana officinalis, 17312-431 — Allium cepa, Arsenicum album, Bryonia alba, Eupatorium perfoliatum, Gelsemium sempervirens, Natrum muriaticum, Nux vomica, Silicea, Sulphur, Zincum gluconicum, 17312-433 — Bryonia alba, Hydrastis canadensis, Kali bichromicum, Natrum Muriaticum, Pulsatilla pratensis, Silicea, Stannum metallicum, Thuja occidentalis, Zincum gluconicum, 17312-477 — Candida Albicans, Wood Creosote, Sodium Chloride, Sulphur, 17312-478 — Chelidonium, Euphrasia, Kali sulph, Natrum muriaticum, Phosphorus, Physostigma, Sepia, Silicea, 21130-880 — ZINC GLUCONATE, 21130-881 — ZINC GLUCONATE, 21130-984 — SODIUM BICARBONATE, SODIUM CHLORIDE, 24208-276 — sodium chloride, 24208-277 — sodium chloride, 24208-385 — sodium chloride, 24330-110 — Calendula Officinalis, Echinacea Angustifolia, Cantharis Vesicatoria, +1752 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.