NDC 53217-004 New Terocin

NDC Product Code 53217-004

NDC 53217-004-01

Package Description: 120 mL 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

New Terocin with NDC 53217-004 is a product labeled by Aidarex Pharmaceuticals Llc. The generic name of New Terocin is . The product's dosage form is and is administered via form.

Labeler Name: Aidarex Pharmaceuticals Llc

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)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • CETYL ALCOHOL (UNII: 936JST6JCN)
  • STEARIC ACID (UNII: 4ELV7Z65AP)
  • GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
  • PEG-100 STEARATE (UNII: YD01N1999R)
  • DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
  • LIDOCAINE (UNII: 98PI200987)
  • LAVENDER OIL (UNII: ZBP1YXW0H8)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • BORAGE OIL (UNII: F8XAG1755S)
  • INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)
  • XANTHAN GUM (UNII: TTV12P4NEE)
  • TROLAMINE (UNII: 9O3K93S3TK)
  • METHYLPARABEN (UNII: A2I8C7HI9T)
  • PROPYLPARABEN (UNII: Z8IX2SC1OH)
  • DMDM HYDANTOIN (UNII: BYR0546TOW)
  • IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)

Product Labeler Information

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

Labeler Name: Aidarex Pharmaceuticals Llc
Labeler Code: 53217
Start Marketing Date: 03-13-2013 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 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.

New Terocin Product Label Images

New Terocin 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

Methyl Salicylate 25%Capsaicin 0.025%Menthol 10%

Purpose

Topical Analgesic

Uses

Temporarily relieves mild aches and pains of muscles or joints.

Warnings

  • Only for external use.Do not use: on open wounds, cuts, damaged or infected skin as well as in the eyes, mouth, genitals, or any other mucous membranes.Consult your physician: if pain is persistent or worsens or if using any other topical pain products.Call poison control if swallowed. If contact with the eyes occurs, rinse eyes thoroughly with cold water.

Keep Out Of Reach Of Children.

Consult physician for children under 12.

Directions

Wash and dry affected area. Shake bottle well before each use and gently rubover area of pain. Use is not recommended more than four times a day. Washhands immediately afterwards to avoid contact with eyes.

Inactive Ingredients

Water (Aqua), Cetyl Alcohol, Stearic Acid, Glyceryl Stearate, PEG-100 Stearate, Propylene Glycol, Dimethyl Sulfone, Lavandula Angustifolia (Lavendar) Oil, Lidocaine, Aloe Barbadensis Leaf Extract, Borago Officinalis Seed Oil, Boswellia Serrata Extract, Xanthan Gum, Triethanolamine, Methylparaben, Propylparaben, DMDM Hydantoin, Iodopropynyl Butylcarbamate.

* Please review the disclaimer below.