NDC 58466-024 Nanocare

  1. Labeler Index
  2. Deramzone Solutions, Inc.
  3. NDC: 58466-024 Nanocare

NDC Product Code 58466-024

NDC CODE: 58466-024

Proprietary Name: Nanocare 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

  • 58466 - Deramzone Solutions, Inc.

NDC 58466-024-24

Package Description: 118 mL in 1 JAR

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

NDC Product Information

Nanocare with NDC 58466-024 is a product labeled by Deramzone Solutions, Inc.. 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: 200010.

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)
  • MINERAL OIL (UNII: T5L8T28FGP)
  • PETROLATUM (UNII: 4T6H12BN9U)
  • ALCOHOL (UNII: 3K9958V90M)
  • GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
  • PEG-100 STEARATE (UNII: YD01N1999R)
  • PARAFFIN (UNII: I9O0E3H2ZE)
  • CETYL ALCOHOL (UNII: 936JST6JCN)
  • IMIDUREA (UNII: M629807ATL)
  • METHYLPARABEN (UNII: A2I8C7HI9T)
  • PROPYLPARABEN (UNII: Z8IX2SC1OH)
  • TROLAMINE (UNII: 9O3K93S3TK)

Product Labeler Information

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

Labeler Name: Deramzone Solutions, Inc.
Labeler Code: 58466
Start Marketing Date: 10-15-2012 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.

Nanocare Product Label Images

Nanocare 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

Other

Drug Facts

Manufactured by:Dermazone Solutions, Inc.2440 30th Avenue North St. Petersburg, FL 33713 USADistributed by: Universal Sales & Marketing, Inc.

Active Ingredients

Dimethicone 1.0%

Purpose

Skin protectant

Uses

  • Helps prevent and relieve chafed or cracked skin

Otc - Do Not Use

For external use only.

Otc - When Using

When using this product keep out of eyes.

Do Not Use On

  • Deep woundsanimal bitesserious burns

Stop Use And Ask A Doctor If

  • Condition worsenssymptoms lasts more than seven days or clear up and occur again within a few days

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Apply to dry areas as neededchildren under 6 months: Ask a doctor

Inactive Ingredients

USP water, mineral oil, petrolatum, alcohol, glyceryl stearate, PEG-100 stearate, paraffin, cetyl alcohol, lecithin, essential oils, imidazolidinyl urea, methylparaben, propylparaben, triethanolamine

* Please review the disclaimer below.