NDC 27281-007 Diabetigen

NDC Product Code 27281-007

NDC 27281-007-96

Package Description: 30 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

Diabetigen with NDC 27281-007 is a product labeled by Sunway Biotech Llc. The generic name of Diabetigen is . The product's dosage form is and is administered via form.

Labeler Name: Sunway Biotech Llc

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)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • WATER (UNII: 059QF0KO0R)

Product Labeler Information

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

Labeler Name: Sunway Biotech Llc
Labeler Code: 27281
Start Marketing Date: 12-09-2013 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: 12-31-2017 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.

Diabetigen Product Label Images

Diabetigen 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

Active Ingredients: Equal volumes of each ingredient: Arnica 3X HPUS, Arsenicum Alb 200C HPUS, DNA 6X HPUS, Echinacea 3X HPUS, Hamamelis 3X HPUS, Helonias 3X HPUS, Hepar Suis 6X HPUS, Iris Vers 6X HPUS, Pancreas Suis 6X HPUS, Phosphoricum Ac 200C HPUS, Rosmarinus 3X HPUS, Secale 30C HPUS, Syzygium 3X HPUS, Uranium Nitricum 30C HPUS.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.

Otc - Purpose

NDC #: 2728100796DIABETIGENEnergy Medicine with DNAHomeopathic Fast-Acting Oral Spray1.0 Fl. Oz. (30 mL)Alcohol 9% v/v

Indications & Usage

Indications:  Temporarily relieves symptoms associated with type II diabetes, including: pancreatic deficiency; liver weakness; apathy and generalized feelings of weakness.

Dosage & Administration

Directions: Take as directed by your health care professional. Standard dosage: Adults and children over 12: Spray twice under the tongue, three times a day. Children under 12: Consult a doctor prior to use.

Warnings

Warnings: Keep out of reach of children. If pregnant or breast feeding, ask a doctor before using product. Stop use and ask a doctor if symptoms persis more than 3 days, worsen, or if new symptoms occur.

Other Safety Information

Tamper Evident Seal: Do not use if seal around neck of bottle is broken or missing. The letters HPUS indicate that ingredients are officially included in the Homeopathic Pharmacopoeia of the United States.Distributed by:SUNWAY BIOTECH LLCOak HIlls, CA 92344 U.S.A. [email protected]

Inactive Ingredient

Inactive Ingredients: Alcohol 9% v/v, Glycerin 10% v/v, Purified Water.

* Please review the disclaimer below.