NDC 55264-001 Shopko Hydrocortisone

NDC Product Code 55264-001

NDC CODE: 55264-001

Proprietary Name: Shopko Hydrocortisone 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

  • 55264 - United Exchange Corp.

NDC 55264-001-86

Package Description: 1 TUBE in 1 CARTON > 28 g in 1 TUBE

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

NDC Product Information

Shopko Hydrocortisone with NDC 55264-001 is a product labeled by United Exchange Corp.. 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: 106258.

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.

  • GLYCERIN (UNII: PDC6A3C0OX)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • SODIUM CHLORIDE (UNII: 451W47IQ8X)
  • PETROLATUM (UNII: 4T6H12BN9U)
  • CETYL ALCOHOL (UNII: 936JST6JCN)
  • DIMETHICONE (UNII: 92RU3N3Y1O)
  • ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
  • DISTEARYLDIMONIUM CHLORIDE (UNII: OM9573ZX3X)
  • METHYLPARABEN (UNII: A2I8C7HI9T)
  • PROPYLPARABEN (UNII: Z8IX2SC1OH)
  • 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: United Exchange Corp.
Labeler Code: 55264
Start Marketing Date: 02-08-2011 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".

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Information for Patients

Hydrocortisone Topical

Hydrocortisone Topical is pronounced as (hye droe kor' ti sone)

Why is hydrocortisone topical medication prescribed?
Hydrocortisone is available with or without a prescription. Low-strength preparations (0.5% or 1%) are used without a prescription for the temporary relief of (1) minor s...
[Read More]

* Please review the disclaimer below.

Shopko Hydrocortisone Product Label Images

Shopko Hydrocortisone 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 Ingredient                                                                                      PurposeHydrocortisone 1% .................................................................................Anti-itch

Otc - Purpose

  • Uses  for the temporary relief of itching associated with minor skin irritations, inflammation and rashes due to:eczemaseborrheic dematitispsoriasisinsect bitespoison ivy, oak, sumacsoapsdetergentscosmeticsjewelryexternal genital, feminine and anal itching

Otc - When Using

Other uses or the use of this product for more than 7 days should be undertaken only under the advice and supervision of a doctor

Warnings

  • Warningsfor external use onlyavoid contact with eyes

Otc - Stop Use

  • Stop using this product and ask a doctorif condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few daysbefore you begin using any other hydrocortisone product

Otc - Ask Doctor

  • Do not use this product and ask a doctorif you have a vaginal dischargebefore treating diaper rashbefore using on children under 2 years of age

Otc - Keep Out Of Reach Of Children

Keep this and all drugs out of the reach of children.If swallowed, get medical help or contact a Poison Control Center right away.Before using any medication, read all label directions.  Keep this carton.  It contains important information.

Indications & Usage

  • Directionsfor adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times dailychildren under 2 years of age: do not use, consult a doctor

Safe Handling Warning

  • Other informationstore at room temperatureLot No. and Exp. Date: see box or see crimp of tube

Inactive Ingredient

Inactive ingredientsglycerin, propylene glycol, sodium chloride, white petrolatum, cetyl alcohol, dimethicone, isopropyl palmitate, distearyldimonium chloride, methylparaben, propylparaben, purified water

Dosage & Administration

Distributed by: United Exchange Corp.17211 Valley View Ave.Cerritos, CA 90703www.ueccorp.comMade in Korea

* Please review the disclaimer below.