NDC 61045-0002 Arthronew PM

NDC Product Code 61045-0002

NDC 61045-0002-1

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

Arthronew PM with NDC 61045-0002 is a product labeled by Purecore Wellness, Inc. The generic name of Arthronew PM is . The product's dosage form is and is administered via form.

Labeler Name: Purecore Wellness, Inc

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.

  • CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
  • ASCORBIC ACID (UNII: PQ6CK8PD0R)
  • HARPAGOPHYTUM PROCUMBENS ROOT (UNII: 1OYM338E89)
  • EDETATE DISODIUM (UNII: 7FLD91C86K)
  • .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
  • OREGANO (UNII: 0E5AT8T16U)
  • POLYETHYLENE GLYCOL 1500 (UNII: 1212Z7S33A)
  • PEG-8 DIMETHICONE (UNII: GIA7T764OD)
  • POLYETHYLENE GLYCOL 700 (UNII: 762678AC5R)
  • MENTHA PIPERITA LEAF (UNII: A389O33LX6)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • CAPRYLYL GLYCOL (UNII: 00YIU5438U)
  • SORBIC ACID (UNII: X045WJ989B)
  • POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
  • WATER (UNII: 059QF0KO0R)
  • SODIUM HYDROXIDE (UNII: 55X04QC32I)
  • SALIX ALBA BARK (UNII: 205MXS71H7)
  • HAMAMELIS VIRGINIANA BARK (UNII: IH3063S9MY)

Product Labeler Information

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

Labeler Name: Purecore Wellness, Inc
Labeler Code: 61045
Start Marketing Date: 11-03-2014 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.

Arthronew PM Product Label Images

Arthronew PM 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 Ingredients:

ARNICA MONTANA 6X, 12X,  HAMAMELIS VIRGINIANA 6X, 12X,  RHUS TOXICODENDRON 6X, 12X

Indications:

For temporary relief of minor symptoms of joint pain and inflammation.

For temporary relief of minor symptoms of joint pain and inflammation.

Warnings:

For external use only. If pregnant or breastfeeding, ask a health professional before use.Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.When using this product - Do not get into eyes. Stop use and consult a doctor if condition worsens.

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.

Directions:

Apply over the affected area once in the evening. Consult a physician for use in children under 12 years of age.

Inactive Ingredients:

ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, ALOE BARBADENSIS LEAF JUICE, ARNICA (FLOWER), ASCORBIC ACID, DEVIL'S CLAW (ROOT), EDETATE DISODIUM (EDTA), MIXED TOCOPHEROLS [VITAMIN E] (DERIVED FROM SOY BEAN), NATURAL PLANT EXTRACT, PEG-33, PEG-8 DIMETHICONE, PEG-14, PEPPERMINT (LEAF), PHENOXYETHANOL, CAPRYLYL GLYCOL, SORBIC ACID, POTASSIUM SORBATE, PURIFIED WATER, SODIUM HYDROXIDE, WHITE WILLOW (BARK), WITCH HAZEL (BARK)

Questions:

Dist. ByPureCore Wellness, Inc.Austin, TX 78733800-448-7442www.ArthroNewProducts.com

Package Label Display:

ARTHRONEWPMHOMEOPATHICJOINT RELIEFNet wt. 2 oz. (57 g)

* Please review the disclaimer below.