NDC 55301-044 Exchange Select Burn Relief Pain Relieving

  1. Labeler Index
  2. Army And Air Force Exchange Service
  3. NDC: 55301-044 Exchange Select Burn Relief Pain Relieving

NDC Product Code 55301-044

NDC CODE: 55301-044

Proprietary Name: Exchange Select Burn Relief Pain Relieving 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

  • 55301 - Army And Air Force Exchange Service

NDC 55301-044-16

Package Description: 227 g in 1 BOTTLE, PLASTIC

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

NDC Product Information

Exchange Select Burn Relief Pain Relieving with NDC 55301-044 is a product labeled by Army And Air Force Exchange Service. The generic name of Exchange Select Burn Relief Pain Relieving is . The product's dosage form is and is administered via form.

Labeler Name: Army And Air Force Exchange Service

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)
  • TROLAMINE (UNII: 9O3K93S3TK)
  • ISOPROPYL ALCOHOL (UNII: ND2M416302)
  • EDETATE DISODIUM (UNII: 7FLD91C86K)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • POLYSORBATE 80 (UNII: 6OZP39ZG8H)
  • DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
  • MENTHOL (UNII: L7T10EIP3A)

Product Labeler Information

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

Labeler Name: Army And Air Force Exchange Service
Labeler Code: 55301
Start Marketing Date: 11-15-2012 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: 12-31-2018 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.

Exchange Select Burn Relief Pain Relieving Product Label Images

Exchange Select Burn Relief Pain Relieving 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

Active Ingredient

Lidocaine HCl 0.50%

Purpose

Topical Analgesic

Uses

  • Temporary relief of pain and itchinghelps relieve and soothes pain from sunburn, minor burns, cuts, scrapes, skin irritations and insect bites

Warnings

For external use onlyDo not use in large quantities, particularly over raw surfaces or blistered areas.

When Using This Product

  • Avoid contact with eyes.

Stop Use And Ask A Doctor If

  • Conditions worsens or symptoms persists for more than 7 days.symptoms clear up and occur again within a few days.

Keep Out Of Reach Of Children.

If swallowed get medical help or contact a Poison Control Center right away.

Directions

  • 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, ask a doctor.

Inactive Ingredients

Water, Propylene Glycol, Glycerin, Isopropyl Alcohol, Triethanolamine, Polysorbate 80, Carbomer, Aloe Barbadensis Leaf Juice Powder, Menthol, Disodium EDTA, Diazolidinyl Urea, Yellow 5, Blue 1.

* Please review the disclaimer below.