NDC 55714-1103 Swimmers Support

Antimon. Tart., Arnica, Bellis, Bryonia, Calc. Carb., Capsicum, Chelidonium Majus, Cuprum Met., Digitalis, Drosera, Lachesis, Lacticum Acidum, Ledum, Mag. Carb., Mang. Acet., Nux Vom., Phytolacca, Rhus Toxicodendron, Ruta, Sarcolacticum Ac., Sulphuricum Ac., Verbascum, Vipera Berus

NDC Product Code 55714-1103

NDC Code: 55714-1103

Proprietary Name: Swimmers Support What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Antimon. Tart., Arnica, Bellis, Bryonia, Calc. Carb., Capsicum, Chelidonium Majus, Cuprum Met., Digitalis, Drosera, Lachesis, Lacticum Acidum, Ledum, Mag. Carb., Mang. Acet., Nux Vom., Phytolacca, Rhus Toxicodendron, Ruta, Sarcolacticum Ac., Sulphuricum Ac., Verbascum, Vipera Berus What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

  • 55714 - Newton Laboratories, Inc.
    • 55714-1103 - Swimmers Support

NDC 55714-1103-0

Package Description: .5 mL in 1 BOTTLE, GLASS

NDC 55714-1103-1

Package Description: 29.57 mL in 1 BOTTLE, GLASS

NDC 55714-1103-2

Package Description: 59.14 mL in 1 BOTTLE, GLASS

NDC Product Information

Swimmers Support with NDC 55714-1103 is a a human over the counter drug product labeled by Newton Laboratories, Inc.. The generic name of Swimmers Support is antimon. tart., arnica, bellis, bryonia, calc. carb., capsicum, chelidonium majus, cuprum met., digitalis, drosera, lachesis, lacticum acidum, ledum, mag. carb., mang. acet., nux vom., phytolacca, rhus toxicodendron, ruta, sarcolacticum ac., sulphuricum ac., verbascum, vipera berus. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Newton Laboratories, Inc.

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

Product Type: Human Otc Drug What kind of product is this?
Indicates 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.

Swimmers Support Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • 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
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE 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 ROTUNDIFOLIA FLOWERING TOP 10 [hp_X]/mL
  • LACHESIS MUTA VENOM 10 [hp_X]/mL
  • LACTIC ACID, DL- 10 [hp_X]/mL
  • LEDUM PALUSTRE TWIG 10 [hp_X]/mL
  • MAGNESIUM CARBONATE 10 [hp_X]/mL
  • MANGANESE ACETATE TETRAHYDRATE 10 [hp_X]/mL
  • STRYCHNOS NUX-VOMICA SEED 10 [hp_X]/mL
  • PHYTOLACCA AMERICANA ROOT 10 [hp_X]/mL
  • TOXICODENDRON PUBESCENS LEAF 10 [hp_X]/mL
  • RUTA GRAVEOLENS FLOWERING TOP 10 [hp_X]/mL
  • LACTIC ACID, L- 10 [hp_X]/mL
  • SULFURIC ACID 10 [hp_X]/mL
  • VERBASCUM THAPSUS 10 [hp_X]/mL
  • VIPERA BERUS VENOM 10 [hp_X]/mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • ALCOHOL (UNII: 3K9958V90M)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Newton Laboratories, Inc.
Labeler Code: 55714
Marketing Category: UNAPPROVED HOMEOPATHIC - What is the Marketing Category?
Product 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.

Start Marketing Date: 03-01-2011 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2018 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: E What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Swimmers Support Product Label Images

Swimmers Support Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Indications & Usage Section

Swimmers Support   Formulated for symptoms associated with swimming and exposure to pool chemicals such as cramping, dry skin, fatigue and muscle soreness.

Dosage & Administration Section

Directions: ORAL USE ONLY - SHAKE WELL.    Ages 12 and up, take 6 drops orally (ages 0 to 11, give 3 drops) as needed or as directed by a healthcare professional. Sensitive persons begin with 1 drop and gradually increase to full dose .

Otc - Active Ingredient Section

Antimon. tart. 10x, Arnica 10x, Bellis 10x, Bryonia 10x, Calc. carb. 10x, Capsicum 10x, Chelidonium majus 10x, Cuprum met. 10x, Digitalis 10x, Drosera 10x, Lachesis 10x, Lacticum acidum 10x, Ledum 10x, Mag. carb. 10x, Mang. acet. 10x, Nux vom.10x, Phytolacca 10x, Rhus toxicodendron 10x, Ruta 10x, Sarcolacticum ac. 10x, Sulphuricum ac. 10x, Verbascum 10x, Vipera berus 10x.

Otc - Purpose Section

Formulated for symptoms associated with swimming and exposure to pool chemicals such as cramping, dry skin, fatigue and muscle soreness.

Inactive Ingredient Section

Inactive Ingredients: USP Purified Water; USP Gluten-free, non-GMO, organic cane dispensing alcohol 20%.

Questions Section

Www.newtonlabs.net Newton Laboratories, Inc. FDA Est # 1051203 - Conyers, GA 30012Questions?  1.800.448.7256

Warnings Section

Warning: Do not use if tamper - evident seal is broken or missing. Consult a licensed healthcare professional if pregnant, nursing or if symptoms worsen or persist for more than a few days. Keep out of reach of children.

Otc - Pregnancy Or Breast Feeding Section

Consult a licensed healthcare professional if pregnant, nursing or if symptoms worsen or persist for more than a few days.

Otc - Keep Out Of Reach Of Children Section

Keep out of reach of children.

* Please review the disclaimer below.

Previous Code
55714-1102
Next Code
55714-1104