NDC 65923-120 Coralite Pain Relief Stick

NDC Product Code 65923-120

NDC CODE: 65923-120

Proprietary Name: Coralite Pain Relief Stick 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

  • 65923 - United Exchange Corp.

NDC 65923-120-01

Package Description: 57 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

Coralite Pain Relief Stick with NDC 65923-120 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: 1248343.

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.

  • METHYL ALCOHOL (UNII: Y4S76JWI15)
  • HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
  • PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • SODIUM STEARATE (UNII: QU7E2XA9TG)
  • 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: 65923
Start Marketing Date: 02-10-2016 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.

Coralite Pain Relief Stick Product Label Images

Coralite Pain Relief Stick 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 ingredients                                                           PurposeMethol 4%.......................................................Topical analgesicMethyl salicylate 1%.........................................Topical analgesic

Otc - Purpose

  • UsesFor temporary relief of minor muscle and joint discomfort associated with:simple backachearthritisstrainsbruisessprains

Warnings

WarningsFor external use only. If pregnant or breast-feeding, ask a health professional before use.Allergy Alert: Do not use if allergic to salicylates (including aspirin) without consulting a physician.

Otc - When Using

When using this product use only as directed, do not bandage tightly or use with a heating pad, avoid contact with eyes and mucous membranes, do not apply to wounds or damaged skin.

Otc - Stop Use

Stop use and ask a doctor if condition worsens, symptoms persist for more than 7 days or clear up and occur again within a few days, redness is present or irritation develops.

Otc - Keep Out Of Reach Of Children

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

Indications & Usage

  • DirectionsAdults and Children 10 Years of Age and OlderApply generously to affected areaMassage into area until thoroughly absorbed into skinRepeat as necessary, but no more than 4 times dailyChildreun Under 10 Years of Age Consult a doctor

Storage And Handling

  • Other informationStore at 20° to 25°C (68° to 77°F)

Inactive Ingredient

Inactive ingredients ethyl alcohol, hydrogenated castor oil, PEG-150 distearate, propylene glycol, sodium stearate, water

Dosage & Administration

Distributed by:United Exchange Corp.17211 Valley View Ave.Cerritos, CA 90703 USAwww.ueccorp.comToll Free: 1 800 814 8028Made in China

* Please review the disclaimer below.