NDC 43074-112 Diabecline

NDC Product Code 43074-112

NDC CODE: 43074-112

Proprietary Name: Diabecline 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

  • 43074 - Phillips Company

NDC 43074-112-11

Package Description: 3 g in 1 BOTTLE

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

NDC Product Information

Diabecline with NDC 43074-112 is a product labeled by Phillips Company. The product's dosage form is and is administered via form. The RxNorm Crosswalk for this NDC code indicates multiple RxCUI concepts are associated to this product: 1542813 and 1542815.

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.

  • ASCORBIC ACID (UNII: PQ6CK8PD0R)
  • CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E)
  • CHOLECALCIFEROL (UNII: 1C6V77QF41)
  • DIMETHYL SULFOXIDE (UNII: YOW8V9698H)
  • DIPROPYLENE GLYCOL (UNII: E107L85C40)
  • GLUCONOLACTONE (UNII: WQ29KQ9POT)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • HYDROXYMETHYL CELLULOSE (UNII: 273FM27VK1)
  • MAGNESIUM STEARATE (UNII: 70097M6I30)
  • METHYLPARABEN (UNII: A2I8C7HI9T)
  • SODIUM HYDROXIDE (UNII: 55X04QC32I)
  • SORBIC ACID (UNII: X045WJ989B)
  • STEARIC ACID (UNII: 4ELV7Z65AP)
  • 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: Phillips Company
Labeler Code: 43074
Start Marketing Date: 06-10-2013 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: 12-31-2019 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.

Diabecline 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

Active Ingredient (In Each Gram)

Tetracycline hydrochloride 30 mg

Purpose

PurposeFirst Aid Antibiotic

Use

First aid to help prevent skin infection in minor cuts, scrapes, and burns.

Warnings

For external use only. May be harmful if swallowed.Allergy alert: Do not use if allergic to any ingredient listed on this label.

Do Not Use

In the eyes. over large areas of the body.longer than 1 week unless directed by doctor.

Ask A Doctor Before Use If You Have

Deep or puncture wounds  animal bites  serious burns

Stop Use And Ask A Doctor

If condition persists or gets worse.

Keep Out Of Reach Of Children

If swallowed, get medical help or contact aPoison Control Center right away.

Directions

Clean the affected area.  Apply a small amount of this product (an amountequal to the surface area of the tip of a finger) on the area 1 to 3 times daily. May be covered with a sterile bandage.

Other Information

Keep product refrigerated to preserve its effectiveness and color. Stop use if product is misused: If the bottle is left open and/or if not refrigerated, the liquid will tend to turn black over time. Discard the product if the liquid turns black due to misuse. This product is an OTC antibiotic for human use. Contains no alcohol, no animal ingredients. Blended for typical skin color. May stain cloth. No claims regarding stem cell healing are implied for this product.

Inactive Ingredients

ASCORBIC ACID, CHLORHEXIDINE GLUCONATE, CHOLECALCIFEROL,DIMETHYL SULFOXIDE, DIPROPYLENE GLYCOL, GLUCONO DELTALACTONE, GLYCERIN, HYDROXETHYLCELLULOSE, MAGNESIUMSTEARATE, METHYLPARABEN, SODIUM HYDROXIDE, SORBIC ACID,STEARIC ACID, WATER

* Please review the disclaimer below.