NDC 50499-300 Dr Mineral Anti-itch

NDC Product Code 50499-300

NDC CODE: 50499-300

Proprietary Name: Dr Mineral Anti-itch 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

  • 50499 - Mineralbio

NDC 50499-300-10

Package Description: 100 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

Dr Mineral Anti-itch with NDC 50499-300 is a product labeled by Mineralbio. The product's dosage form is and is administered via form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 1044248.

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)
  • GLYCERIN (UNII: PDC6A3C0OX)

Product Labeler Information

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

Labeler Name: Mineralbio
Labeler Code: 50499
Start Marketing Date: 02-20-2010 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.

Dr Mineral Anti-itch Product Label Images

Dr Mineral Anti-itch 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 - Purpose

[Uses]Dr. Mineral Anti-Itch Spray is useful for the temporary relief of itching associated with irritation, rashes and inflammation due to- skin dryness - eczema - psoriasis - photo sensitivity - jewelry - insect bites - soaps and detergents - cosmetics - poison ivy, oak or sumac - seborrheic dermattis - Other use of this product ask a doctor

Otc - When Using

[Directions]Apply when needed not more than 5-6 times a day.- spray 2-3 times when use- Children under 2 years, do not use: ask a doctor

Warnings

[Warnings] For external use only.- Do not use in or near the eyes.  For diaper rash: ask a doctor- Stop use and ask a doctor if      - condition worsens      - symtoms persist for more than 7 days or clear up and occur again within a few days

Otc - Keep Out Of Reach Of Children

Keep out of reach of the children.  If swallowed, get medical help or contact a Poison Control Center immediately.

Otc - Active Ingredient

[Active Ingredients} Sodium Chloride 0.7%, Menthol 0.05%

Storage And Handling

[Storage]Store at a room temperature.  Protect from freezing and excessive heat.Expire: 02.25.2012

Inactive Ingredient

[Inactive Ingredients] Water, Glycerin, Grapefruit Seed Extract, Zinc Chloride, Cupric Chloride, Germanium Dioxide, Ethanol, Polysorbate 20

* Please review the disclaimer below.