NDC 68703-338 N-con Tonic

Calc Fluor, Equisetum Arv, Nat Phos, Nat Sulphuricum, Pulsatilla

NDC Product Code 68703-338

NDC Code: 68703-338

Proprietary Name: N-con Tonic 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: Calc Fluor, Equisetum Arv, Nat Phos, Nat Sulphuricum, Pulsatilla 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.

Product Characteristics

Color(s):
WHITE (C48325 - ROUND LACTOSE TABLET)
Shape: ROUND (C48348)
Size(s):
6 MM
Imprint(s):
NONE
Score: 1

NDC Code Structure

  • 68703 - Silver Star Brands

NDC 68703-338-30

Package Description: 180 TABLET in 1 BOTTLE, GLASS

NDC Product Information

N-con Tonic with NDC 68703-338 is a a human over the counter drug product labeled by Silver Star Brands. The generic name of N-con Tonic is calc fluor, equisetum arv, nat phos, nat sulphuricum, pulsatilla. The product's dosage form is tablet and is administered via oral form.

Labeler Name: Silver Star Brands

Dosage Form: Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.

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.

N-con Tonic 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.

  • EQUISETUM ARVENSE BRANCH 6 [hp_X]/1
  • CALCIUM FLUORIDE 6 [hp_C]/1
  • SODIUM SULFATE 6 [hp_C]/1
  • SODIUM PHOSPHATE, DIBASIC, UNSPECIFIED FORM 6 [hp_C]/1
  • PULSATILLA VULGARIS 6 [hp_X]/1

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.

  • ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)
  • MAGNESIUM STEARATE (UNII: 70097M6I30)
  • SUCROSE (UNII: C151H8M554)
  • ACACIA (UNII: 5C5403N26O)
  • WATER (UNII: 059QF0KO0R)

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: Silver Star Brands
Labeler Code: 68703
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: 09-09-2019 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: 12-31-2020 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: N 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.

N-con Tonic Product Label Images

N-con Tonic 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

Hpus Active Ingredients

HPUS Active Ingredients: Each dose contains equal parts of: Calc fluor 6C, Equisetum arv 6X, Nat phos 6C, Nat sulphuricum 6C, Pulsatilla 6X.The letters HPUS indicate that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of the United States.

Uses*

Uses*: Homeopathic remedy for common incontinence, bladder strength and urinary system support.*This statement has not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease.

Warnings

Warnings: If symptoms persist or worsen, consult a healthcare professional. If pregnant or breastfeeding, ask a health professional before use. Keep this and all medication out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Directions

Directions; Adults & Children 13+: Take 2 tablets 2-3 times daily as needed. Children 6-12: Take 1-2 tablets 2 times daily as needed. Special instructions: Avoid strong mint flavored candy.

Other Safety Information

Contains no artificial flavors or colorants. No gluten added.Tamper resistant for your protection. Use only if safety seal is intact.

Inactive Ingredients

Inactive Ingredients: Acacia gum, distilled water, lactose, magnesium stearate, sucrose.

Otc - Keep Out Of Reach Of Children

Keep this and all medication out of reach of children.

Otc - Pregnancy Or Breast Feeding

If pregnant or breastfeeding, ask a health professional before use.

Otc - Purpose

Reduces sudden urges & leakages due to incontinence.

* Please review the disclaimer below.