55714-2526 NDC - SWIMMERS FRIEND (ANTIMONIUM TART., ARNICA MONTANA, BELLIS PERENNIS, BRYONIA, CALCAREA CARBONICA, CAPSICUM ANNUUM, CHELIDONIUM MAJUS, CUPRUM METALLICUM, DIGITALIS PURPUREA, DROSERA, LACHESIS MUTUS, LACTICUM ACIDUM, LEDUM PALUSTRE, MAGNESIA CARBONICA, MANGANUM ACETICUM, NUX VOMICA, PHYTOLACCA DECANDRA, RHUS TOXICODENDRON, RUTA GRAVEOLENS, SARCOLACTICUM ACIDUM, SULPHURICUM ACIDUM, VERBASCUM THAPSUS, VIPERA BERUS)

Drug Information

  • Product NDC: 55714-2526
  • Proprietary Name: Swimmers Friend
  • Non Proprietary Name: Antimonium tart., Arnica montana, Bellis perennis, Bryonia, Calcarea carbonica, Capsicum annuum, Chelidonium majus, Cuprum metallicum, Digitalis purpurea, Drosera, Lachesis mutus, Lacticum acidum, Ledum palustre, Magnesia carbonica, Manganum aceticum, Nux vomica, Phytolacca decandra, Rhus toxicodendron, Ruta graveolens, Sarcolacticum acidum, Sulphuricum acidum, Verbascum thapsus, Vipera berus
  • Active Ingredient(s): 10 [hp_X]/mL ANTIMONY POTASSIUM TARTRATE; 10 [hp_X]/mL ARNICA MONTANA; 10 [hp_X]/mL BELLIS PERENNIS; 10 [hp_X]/mL BRYONIA ALBA ROOT; 10 [hp_X]/mL CAPSICUM; 10 [hp_X]/mL CHELIDONIUM MAJUS; 10 [hp_X]/mL COPPER; 10 [hp_X]/mL DIGITALIS; 10 [hp_X]/mL DROSERA ANGLICA; 10 [hp_X]/mL LACHESIS MUTA VENOM; 10 [hp_X]/mL LACTIC ACID, DL-; 10 [hp_X]/mL LACTIC ACID, L-; 10 [hp_X]/mL MAGNESIUM CARBONATE; 10 [hp_X]/mL MANGANESE ACETATE TETRAHYDRATE; 10 [hp_X]/mL OYSTER SHELL CALCIUM CARBONATE, CRUDE; 10 [hp_X]/mL PHYTOLACCA AMERICANA ROOT; 10 [hp_X]/mL RHODODENDRON TOMENTOSUM LEAFY TWIG; 10 [hp_X]/mL RUTA GRAVEOLENS FLOWERING TOP; 10 [hp_X]/mL STRYCHNOS NUX-VOMICA SEED; 10 [hp_X]/mL SULFURIC ACID; 10 [hp_X]/mL TOXICODENDRON PUBESCENS LEAF; 10 [hp_X]/mL VERBASCUM THAPSUS; 10 [hp_X]/mL VIPERA BERUS VENOM
  • Administration Route(s): ORAL
  • Dosage Form(s): LIQUID
  • Pharmacy Class(es): Allergens [CS]; Allergens [CS]; Cell-mediated Immunity [PE]; Cell-mediated Immunity [PE]; Copper [CS]; Copper-containing Intrauterine Device [EPC]; Decreased Embryonic Implantation [PE]; Decreased Sperm Motility [PE]; Dietary Proteins [CS]; Increased Histamine Release [PE]; Increased Histamine Release [PE]; Increased IgG Production [PE]; Inhibit Ovum Fertilization [PE]; Magnetic Resonance Contrast Activity [MoA]; Non-Standardized Food Allergenic Extract [EPC]; Non-Standardized Plant Allergenic Extract [EPC]; Non-Standardized Plant Allergenic Extract [EPC]; Paramagnetic Contrast Agent [EPC]; Plant Proteins [CS]; Plant Proteins [CS]; Seed Storage Proteins [CS]; Vegetable Proteins [CS]

Labeler Information

Field Name Field Value
Labeler Name: Newton Laboratories, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:1/1/2019

Package Information

No. Package Code Package Description Billing Unit
155714-2526-130 mL in 1 BOTTLE, GLASS (55714-2526-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC55714-2526The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAMESwimmers FriendThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEAntimonium tart., Arnica montana, Bellis perennis, Bryonia, Calcarea carbonica, Capsicum annuum, Chelidonium majus, Cuprum metallicum, Digitalis purpurea, Drosera, Lachesis mutus, Lacticum acidum, Ledum palustre, Magnesia carbonica, Manganum aceticum, Nux vomica, Phytolacca decandra, Rhus toxicodendron, Ruta graveolens, Sarcolacticum acidum, Sulphuricum acidum, Verbascum thapsus, Vipera berusThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMELIQUIDThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEORALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE1/1/2019This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED HOMEOPATHICProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAMENewton Laboratories, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEANTIMONY POTASSIUM TARTRATE; ARNICA MONTANA; BELLIS PERENNIS; BRYONIA ALBA ROOT; CAPSICUM; CHELIDONIUM MAJUS; COPPER; DIGITALIS; DROSERA ANGLICA; LACHESIS MUTA VENOM; LACTIC ACID, DL-; LACTIC ACID, L-; MAGNESIUM CARBONATE; MANGANESE ACETATE TETRAHYDRATE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PHYTOLACCA AMERICANA ROOT; RHODODENDRON TOMENTOSUM LEAFY TWIG; RUTA GRAVEOLENS FLOWERING TOP; STRYCHNOS NUX-VOMICA SEED; SULFURIC ACID; TOXICODENDRON PUBESCENS LEAF; VERBASCUM THAPSUS; VIPERA BERUS VENOMAn active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10 
ACTIVE INGRED UNIT[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 
PHARM CLASSESAllergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Inhibit Ovum Fertilization [PE], Magnetic Resonance Contrast Activity [MoA], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Paramagnetic Contrast Agent [EPC], Plant Proteins [CS], Plant Proteins [CS], Seed Storage Proteins [CS], Vegetable Proteins [CS] 

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This page was last updated on: 12/19/2025

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