NDC 21130-764 Pain Relief Roller Signature Care

NDC Product Code 21130-764

NDC 21130-764-03

Package Description: 73 mL in 1 BOTTLE

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

NDC Product Information

Pain Relief Roller Signature Care with NDC 21130-764 is a product labeled by Better Living. The generic name of Pain Relief Roller Signature Care is . The product's dosage form is and is administered via form.

Labeler Name: Better Living

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.

  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3)
  • ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
  • FRANKINCENSE (UNII: R9XLF1R1WM)
  • CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
  • GREEN TEA LEAF (UNII: W2ZU1RY8B0)
  • CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F)
  • ISOPROPYL ALCOHOL (UNII: ND2M416302)
  • ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
  • MELISSA OFFICINALIS LEAF (UNII: 50D2ZE9219)
  • SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
  • .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
  • TROLAMINE (UNII: 9O3K93S3TK)
  • 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: Better Living
Labeler Code: 21130
Start Marketing Date: 03-30-2018 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.

Pain Relief Roller Signature Care Product Label Images

Pain Relief Roller Signature Care 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

Uses

For the temporary relief from minor aches and pains of soar muscles and joints associated with arthritis, backache, strains and sprains

Inactive Ingredients

Aloe Barbadensis Leaf ExtractArctium Lappa Root (Burdock) ExtractArnica Montana Flower ExtractBoswellia Carterii Resin ExtractCalendula Officinalis ExtractCamellia Sinensis Leaf ExtractCamphorCarbomerFD&C Blue #1FD&C Yellow #5GlycerinIlex Paraguariensis (Mate) Leaf ExtractIsopropyl AlcoholIsopropyl MyristateMelissa Officinalis (Lemon Balm) Leaf ExtractSilicaTocopheryl AcetateTriethanolamineWater

* Please review the disclaimer below.