NDC 50845-0218 Joint Pain And Stiffness Relief

NDC Product Code 50845-0218

NDC 50845-0218-1

Package Description: 30 mL in 1 BOTTLE, SPRAY

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

NDC Product Information

Joint Pain And Stiffness Relief with NDC 50845-0218 is a product labeled by Liddell Laboratories, Inc.. The generic name of Joint Pain And Stiffness Relief is . The product's dosage form is and is administered via form.

Labeler Name: Liddell Laboratories, 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.

  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
  • LARREA TRIDENTATA TOP (UNII: PK0TXD049P)
  • COMFREY LEAF (UNII: DG4F8T839X)
  • CROTON LECHLERI RESIN (UNII: GGG6W25C63)
  • EGG SHELL MEMBRANE (UNII: N7QBR4212V)
  • LECITHIN, SUNFLOWER (UNII: 834K0WOS5G)
  • LAVANDULA ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M)
  • SILVER (UNII: 3M4G523W1G)
  • MELISSA OFFICINALIS LEAF (UNII: 50D2ZE9219)
  • POLYETHYLENE GLYCOL 1500 (UNII: 1212Z7S33A)
  • PEG-8 DIMETHICONE (UNII: GIA7T764OD)
  • POLYETHYLENE GLYCOL 700 (UNII: 762678AC5R)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • CAPRYLYL GLYCOL (UNII: 00YIU5438U)
  • SORBIC ACID (UNII: X045WJ989B)
  • PHYTOLACCA AMERICANA FRUIT (UNII: WE63661499)
  • PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG)
  • POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
  • WATER (UNII: 059QF0KO0R)
  • SODIUM BICARBONATE (UNII: 8MDF5V39QO)
  • HYPERICUM PERFORATUM (UNII: XK4IUX8MNB)
  • .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
  • ASCORBIC ACID (UNII: PQ6CK8PD0R)
  • WHEY (UNII: 8617Z5FMF6)
  • SALIX ALBA BARK (UNII: 205MXS71H7)
  • ACHILLEA MILLEFOLIUM FLOWER (UNII: YQR8R0SQEA)

Product Labeler Information

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

Labeler Name: Liddell Laboratories, Inc.
Labeler Code: 50845
Start Marketing Date: 01-06-2015 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.

Joint Pain And Stiffness 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

Active Ingredients:

CALENDULA OFFICINALIS 12X, CROTON TIGLIUM 30X, NATRUM MURIATICUM 30X, PLANTAGO MAJOR 30X, RHUS TOX 30X, SARSAPARILLA (SIMILAX REGELII) 30X

Indications:

May temporarily relieve pain due to inflammation caused by but not limited to the following: sprains, minor joint inflammation, trauma.****These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

May temporarily relieve pain due to inflammation caused by but not limited to the following: sprains, minor joint inflammation, trauma.****These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

Warnings:

For external use only.If symptoms persist, consult a doctor.If pregnant or breast-feeding, ask a doctor before use.Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.Do not get into eyes.Do not use if TAMPER EVIDENT seal around neck of bottle is missing or broken.

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:

Adults and children over 12: Spray liberally on affected area as needed. Children 12 and under: Consult a doctor prior to use.

Inactive Ingredients:

ALOE BARBADENSIS LEAF JUICE (ALOE VERA 10X CONCENTRATE), ARNICA MONTANA (FLOWER), LARREA TRIDENTATA (LEAF), SYMPHYTUM OFFICINALE (LEAF), CROTON LECHLERI (SAP), INSTANTIZED SOLUBLE EGGSHELL MEMBRANE + (BIOVADERM BRAND WITH 1% SUNFLOWER LECITHIN), LAVANDULA ANGUSTIFOLIA (BUDS), IONIC COLLOIDAL SILVER, MELISSA OFFICINALIS (LEAF), [PEG-33, PEG-8 DIMETHICONE, PEG-14 (SILSENSE COPOLYOL-1 SILICONE)], [PHENOXYETHANOL, CAPRYLYL GLYCOL, SORBIC ACID, (OPTIPHEN-PLUS)], PHYTOLACCA AMERICANA (BERRIES), PHYTOLACCA AMERICANA (ROOT), POTASSIUM SORBATE, PURIFIED WATER, SODIUM BICARBONATE, HYPERICUM PERFORATUM (AERIAL PARTS), TOCOPHEROL [VITAMIN E OIL] (DERIVED FROM SOY BEAN), VITAMIN C POWDER (ASCORBIC ACID), WHEY PROTEIN CONCENTRATE, SALIX ALBA (BARK), ACHELLEA MILLEFOLIUM (FLOWER)

Questions:

DIST. BY LIDDELL LABORATORIES, INC.   WOODBINE, IA  51579WWW.LIDDELL.NET    1-800-460-7733

Package Label Display:

ORAL SPRAYSLIDDELL LABORATORIESEST. 1994Joint Pain & Stiffness ReliefTOPICAL HOMEOPATHIC SPRAY1.0 FL OZ. (30 ml)

* Please review the disclaimer below.