NDC 57955-1070 Self Abuse

NDC Product Code 57955-1070

NDC CODE: 57955-1070

Proprietary Name: Self Abuse 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.

NDC Code Structure

  • 57955 - King Bio Inc.

NDC 57955-1070-2

Package Description: 59 mL in 1 BOTTLE, SPRAY

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Self Abuse with NDC 57955-1070 is a product labeled by King Bio Inc.. The product's dosage form is and is administered via form.

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)
  • CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
  • POTASSIUM SORBATE (UNII: 1VPU26JZZ4)

Product Labeler Information

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

Labeler Name: King Bio Inc.
Labeler Code: 57955
Start Marketing Date: 08-07-2013 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: I - INACTIVATED, the listing data was inactivated by the FDA. 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.

Self Abuse Product Label Images

Self Abuse 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

Otc - Active Ingredient

Drug Facts____________________________________________________________________________________________________________HPUS active ingredients: ​Agaricus muscarius, Aloe socotrina, Aurum metallicum, Carboneum sulphuratum, Chamomilla, Cimicifuga racemosa, Ilex aquifolium, flos, Lilium tigrinum, Malus pumila, flos, Millefolium, Natrum carbonicum, Pinus sylvestris, flos, Stramonium, Tarentula hispana  Equal volumes of each ingredient in 10X, 30X, 100X, 1M LM1, LM2, LM3 potencies.

Indications & Usage

  • Uses a natural aid for: internalized angerself-contempt and blamedissatisfaction with lifeviolent thoughts/actionsdepressionself-inflicted violence

Inactive Ingredient

Inactive ingredients: Bio-Energetically Enhanced pure water base, citric acid, potassium sorbate.

Warnings

  • WarningsStop use and ask your doctor if symptoms persist or worsen.If pregnant or breast-feeding, take only on advice of a healthcare professional.

Otc - Keep Out Of Reach Of Children

  • Keep out of reach of children.

Dosage & Administration

  • Directions:Initially, depress pump until primed.Spray one dose directly into mouth.Adults: 3 sprays 3 times per day.Children 2-12 years: 2 sprays 3 times per day.Use additionally as needed, up to 6 times per day.

Other Safety Information

Tamper resistant for your protection. Use only if safety seal is intact.

Otc - Purpose

Uses a natural aid for: internalized anger, self-contempt and blame, dissatisfaction with life, violent thoughts/actions, depression, self-inflicted violence.

* Please review the disclaimer below.