"17312-096-19" National Drug Code (NDC)

Dryness Relief Pf 1 BOTTLE, DROPPER in 1 PACKAGE (17312-096-19) / 10 mL in 1 BOTTLE, DROPPER
(TRP Company)

NDC Code17312-096-19
Package Description1 BOTTLE, DROPPER in 1 PACKAGE (17312-096-19) / 10 mL in 1 BOTTLE, DROPPER
Product NDC17312-096
Product Type NameHUMAN OTC DRUG
Proprietary NameDryness Relief Pf
Non-Proprietary NameSilver, Sodium Chloride, Nutmeg, Ruta Graveolens, Sulfur, Zinc
Dosage FormLIQUID
UsageOPHTHALMIC
Start Marketing Date20220809
Marketing Category NameUNAPPROVED HOMEOPATHIC
ManufacturerTRP Company
Substance NameNUTMEG; RUTA GRAVEOLENS FLOWERING TOP; SILVER; SODIUM CHLORIDE; SULFUR; ZINC
Strength12; 8; 10; 6; 9; 12
Strength Unit[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Pharmacy ClassesAllergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Food Additives [CS], Increased Histamine Release [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Osmotic Activity [MoA], Osmotic Laxative [EPC], Plant Proteins [CS], Seed Storage Proteins [CS]

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