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  4. NDC Product Code: 59985-611 Family I Kit

NDC 59985-611 Family I Kit

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 59985-611?
  5. Family I Kit Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

Get all the details for National Drug Code (NDC) 59985-611 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.

NDC Product Code:
59985-611
Proprietary Name:
Family I Kit
Product Type: [3]
Labeler Name: [5]
Chc Montana
Labeler Code:
59985
Product Label ID:
cb59ce94-d0f4-4067-8ea2-c81952de1fb4
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date: [9]
12-30-2015
End Marketing Date: [10]
12-31-2020
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
D
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)

Code Structure Chart

Product Details

What is NDC 59985-611?

The NDC code 59985-611 is assigned by the FDA to the product Family I Kit which is product labeled by Chc Montana. The product's dosage form is . The product is distributed in a single package with assigned NDC code 59985-611-61 46 vial, glass in 1 case / 100 pellet in 1 vial, glass (59985-611-20). This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Family I Kit?

Remember, One Pellet is One Dose!Symphytum (Bone Knit) Take one pellet, three times per day for 2-6 weeks to promote pain relief and rapid healing.EMERGENCIES: For severe pain of internal origin: kidney stone, severe cramp, etc... During transport of emergency, give Belladonna 1 every 5 minutes, 3 times to diminish painFOR EMERGENCY PAIN: CALL 911 OR TRANSPORT TO HOSPITAL.REMEDIES MAY BE USED FOR PAIN EVERY 5 MINS ALONG THE WAY• Arnica: Give for injuries, surgery, head injury or stroke. In emergency, use 1 every 5 minutes 3 times, then hourly 3 times. Arnica is in Injury Combo.• Ledum: Homeopathic Tetanus for pain or puncture wounds and healing. Use 1 dose 3 times in a row.• Hypericum: (Nerve Pain) Shooting pain, smashed fingers and pain of finger and toenails.• Aconite: (For Fright) For shock or hysteria from fright or injury. 1-3 doses in a row should produce calm.• Belladonna: (Violent) Red, hot, throbbing. So violent in nature you need to transport to hospital. Give remedy during transport. High Fevers, pain of horrible things, like migraines. Use every 5 minutes until pain diminishes.• Pyrog: (Sepsis) Poisoning and sepsis bites. When other remedies for poisoning fail. 1 dose every 5 minutes, recheck status hourly for 3 hours and reassess.• Carbo Veg: (Reliever!) Cold, clammy, gasping for air, needs to be fanned, runs to open window to breathe. Faint, shock.• Arsenicum: Illness or poisoning with restlessness and fear of death.• Histaminum: Swelling and itching of hives, bites or minor allergic reactions.• Mercury: Pain in teeth of abscess or decay.Diluting your remedy in water softens the message to balance. Its effect is gentle and easy to use.Fill a 16 oz. bottle halfway with water (about 8 oz.) and drop in one pellet. Dissolve the pellet and shake the bottle well. Label the bottle with the remedy name. You may use this watered down remedy for any irritation or unwanted symptoms in the first week to ten days. Take approximately one teaspoon of this water, swish it in your mouth and hold it for about ten seconds before swallowing.For intense aggravation you may take one teaspoon every five minutes for three times. If the symptom is not resolved, journal it and report it in your follow-up which should be within two weeks of your initial appointment.

Which are Family I Kit UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Family I Kit Inactive Ingredients UNII Codes?

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. The UNII codes for the inactive ingredients in this product are:

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Product Footnotes

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

[8] 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.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[10] What is the End Marketing Date? - This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.

[11] 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.

[12] 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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".