NDC 72186-011 Retreat

Calcium Fluoride, Calcium Phosphate, Unspecified Form, Calcium Sulfate, Unspecified Form, Ferrous Phosphate, Magnesium Phosphate, Tribasic, Pentahydrate, Potassium Chloride, Dibasic Potassium Phosphate, Sodium Chloride, Sodium Phosphate, Sodium Sulfate, Hydrated Silica, And Centaurea Benedicta

NDC Product Code 72186-011

NDC CODE: 72186-011

Proprietary Name: Retreat 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: Calcium Fluoride, Calcium Phosphate, Unspecified Form, Calcium Sulfate, Unspecified Form, Ferrous Phosphate, Magnesium Phosphate, Tribasic, Pentahydrate, Potassium Chloride, Dibasic Potassium Phosphate, Sodium Chloride, Sodium Phosphate, Sodium Sulfate, Hydrated Silica, And Centaurea Benedicta 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

  • 72186 - Key Origins, Inc.

NDC 72186-011-11

Package Description: 30 mL in 1 JAR

NDC Product Information

Retreat with NDC 72186-011 is a a human over the counter drug product labeled by Key Origins, Inc.. The generic name of Retreat is calcium fluoride, calcium phosphate, unspecified form, calcium sulfate, unspecified form, ferrous phosphate, magnesium phosphate, tribasic, pentahydrate, potassium chloride, dibasic potassium phosphate, sodium chloride, sodium phosphate, sodium sulfate, hydrated silica, and centaurea benedicta. The product's dosage form is gel and is administered via topical form.

Labeler Name: Key Origins, Inc.

Dosage Form: Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.

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.

Retreat 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.

  • CALCIUM FLUORIDE 6 [hp_X]/mL
  • CALCIUM PHOSPHATE, UNSPECIFIED FORM 6 [hp_X]/mL
  • CALCIUM SULFATE, UNSPECIFIED FORM 6 [hp_X]/mL
  • FERROUS PHOSPHATE 6 [hp_X]/mL
  • MAGNESIUM PHOSPHATE, TRIBASIC, PENTAHYDRATE 6 [hp_X]/mL
  • POTASSIUM CHLORIDE 6 [hp_X]/mL
  • DIBASIC POTASSIUM PHOSPHATE 6 [hp_X]/mL
  • SODIUM CHLORIDE 6 [hp_X]/mL
  • SODIUM PHOSPHATE 6 [hp_X]/mL
  • SODIUM SULFATE 6 [hp_X]/mL
  • HYDRATED SILICA 6 [hp_X]/mL
  • CENTAUREA BENEDICTA .0231 mg/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.

  • WATER (UNII: 059QF0KO0R)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • PROPANEDIOL (UNII: 5965N8W85T)

Administration Route(s)

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

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

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

Labeler Name: Key Origins, Inc.
Labeler Code: 72186
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: 12-02-2019 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: 12-31-2021 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 - NO 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Retreat 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

Other

RETREAT GEL LABEL:

No contraindications, non-toxic, harmless to humans and animals.

This product is not intended to diagnose, treat, cure, or prevent any disease.

RETREAT SPRAY LABEL:

No contraindications, non-toxic, harmless to humans and animals.

This product is not intended to diagnose, treat, cure, or prevent any disease.

Inactive Ingredient

12 cell minerals, cnicus benedictus, water, organic aloe gel, zemea, and a proprietary blend of 35 interactive ingredients.

12 cell minerals, cnicus benedictus, water, USP grade pharma ethyl alcohol, zemea, and a proprietary blend of 35 interactive ingredients.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.

Keep out of reach of children.

Otc - Purpose

Odor free topical gel for use when traumatized cellular structures are present.

Nutrient rich spray for use when traumatized cellular structures are present.

Directions

Apply to/or directly over the affected area twice daily and apply directly to the bottom of the right foot in the entire arch area twice daily.

Three sprays under the tongue twice daily. Before spraying activate contents by "pounding" bottle in the palm 12 or more times.

* Please review the disclaimer below.