NDC 73596-100 Truu Balance Pain Relief

NDC Product Code 73596-100

NDC CODE: 73596-100

Proprietary Name: Truu Balance Pain Relief 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

  • 73596 - Philia Group Llc

NDC 73596-100-01

Package Description: 1 BOTTLE in 1 BOX > 113 g in 1 BOTTLE

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

NDC Product Information

Truu Balance Pain Relief with NDC 73596-100 is a product labeled by Philia Group Llc. The product's dosage form is and is administered via form.

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)
  • ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
  • C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
  • EMU OIL (UNII: 344821WD61)
  • DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)
  • ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
  • GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)
  • ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
  • LAURETH-7 (UNII: Z95S6G8201)
  • TEA TREE OIL (UNII: VIF565UC2G)
  • DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • STEARIC ACID (UNII: 4ELV7Z65AP)
  • 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: Philia Group Llc
Labeler Code: 73596
Start Marketing Date: 08-17-2020 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: 12-31-2021 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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Truu Balance Pain Relief Product Label Images

Truu Balance Pain Relief 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

Distributed by Philia Group LLCAddress: 4 Flanders Drive, Pine Brook, NJ 07058

Otc - Purpose

Active IngredientsPurposeLidocaine 4% HCl w/wExternal AnalgesicMenthol 1% w/wExternal Analgesic

Uses

For temporary relief of pain, burning, or itching where applied locally

Warnings

For eternal use onlyAvoid contact with eyes

Otc - Do Not Use

Do not use in large quantities, particularly over raw surfaces or blistered areas

Stop Use And Ask Doctor If

  • Condition worsens or if symptoms persist for more than 7 days or clear up and occur again within a few days.

Otc - Keep Out Of Reach Of Children

  • Keep out of reach of childrenIf product is swallowed get medical help or contact a Poison Control Center right away.This product is not intended to diagnose, treat, cure or prevent any disease

Directions

Apply in a circular motion for 30 to 60 secondsFor adults and children two-years and older: apply to affected area not more than 3 to 4 times daily. Children under 2 years of age: consult a physician.

Inactive Ingredients

Aqua (Deionized Water), Arnica Montana Flower Extract, C13-14 Isoparaffin, Chondroitin Sulfate, Emu Oil, Ethoxydiglycol, Ethylhexylglycerin, Glucosamine Sulfate, Isopropyl Palmitate, Laureth-7, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Methylsulfonylmethane (MSM), Phenoxyethanol, Polyacrylamide, Propylene Glycol, Stearic Acid, Triethanolamine, Full Spectrum Hemp Extract. (Aerial Parts)

Other Information

Protect this product from excessive heat and direct sunlight

* Please review the disclaimer below.