NDC 50499-300 Dr Mineral Anti-itch
NDC Product 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.
Non-Proprietary Name: What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
NDC Code Structure
- 50499 - Mineralbio
- 50499-300 - Dr Mineral Anti-itch
NDC 50499-300-10
Package Description: 100 mL in 1 BOTTLE, SPRAY
NDC Product Information
Dr Mineral Anti-itch with NDC 50499-300 is a product labeled by Mineralbio. The generic name of Dr Mineral Anti-itch is . The product's dosage form is and is administered via form.
Dosage Form: -
Product Type: What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
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 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. Values = ‘Y’ or ‘N’.
* 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
- Otc - When Using
- Warnings
- Otc - Keep Out Of Reach Of Children
- Otc - Active Ingredient
- Storage And Handling
- Inactive Ingredient
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.
